Datasets:

MedRAG
/

textbooks

Dataset card Viewer Files Files and versions Community

Split (1)

train · 126k rows

id stringlengths 14 28	title stringclasses 18 values	content stringlengths 2 999	contents stringlengths 19 1.02k
Anatomy_Gray_600	Anatomy_Gray	Large vessels, nerves, and lymphatics are associated with the posterior abdominal wall along the median axis of the body in the region where, during development, the peritoneum reflects off the wall as the dorsal mesentery, which supports the developing gut tube. As a consequence, branches of the neurovascular structures that pass to parts of the gastrointestinal system are unpaired, originate from the anterior aspects of their parent structures, and travel in mesenteries or pass retroperitoneally in areas where the mesenteries secondarily fuse to the wall. Generally, vessels, nerves, and lymphatics to the abdominal wall and to organs that originate as retroperitoneal structures branch laterally from the central neurovascular structures and are usually paired, one on each side.	Anatomy_Gray. Large vessels, nerves, and lymphatics are associated with the posterior abdominal wall along the median axis of the body in the region where, during development, the peritoneum reflects off the wall as the dorsal mesentery, which supports the developing gut tube. As a consequence, branches of the neurovascular structures that pass to parts of the gastrointestinal system are unpaired, originate from the anterior aspects of their parent structures, and travel in mesenteries or pass retroperitoneally in areas where the mesenteries secondarily fuse to the wall. Generally, vessels, nerves, and lymphatics to the abdominal wall and to organs that originate as retroperitoneal structures branch laterally from the central neurovascular structures and are usually paired, one on each side.
Anatomy_Gray_601	Anatomy_Gray	The superior aperture of the abdomen is the inferior thoracic aperture, which is closed by the diaphragm (see pp. 126-127). The margin of the inferior thoracic aperture consists of vertebra TXII, rib XII, the distal end of rib XI, the costal margin, and the xiphoid process of the sternum. The musculotendinous diaphragm separates the abdomen from the thorax. The diaphragm attaches to the margin of the inferior thoracic aperture, but the attachment is complex posteriorly and extends into the lumbar area of the vertebral column (Fig. 4.8). On each side, a muscular extension (crus) firmly anchors the diaphragm to the anterolateral surface of the vertebral column as far down as vertebra LIII on the right and vertebra LII on the left. Because the costal margin is not complete posteriorly, the diaphragm is anchored to arch-shaped (arcuate) ligaments, which span the distance between available bony points and the intervening soft tissues:	Anatomy_Gray. The superior aperture of the abdomen is the inferior thoracic aperture, which is closed by the diaphragm (see pp. 126-127). The margin of the inferior thoracic aperture consists of vertebra TXII, rib XII, the distal end of rib XI, the costal margin, and the xiphoid process of the sternum. The musculotendinous diaphragm separates the abdomen from the thorax. The diaphragm attaches to the margin of the inferior thoracic aperture, but the attachment is complex posteriorly and extends into the lumbar area of the vertebral column (Fig. 4.8). On each side, a muscular extension (crus) firmly anchors the diaphragm to the anterolateral surface of the vertebral column as far down as vertebra LIII on the right and vertebra LII on the left. Because the costal margin is not complete posteriorly, the diaphragm is anchored to arch-shaped (arcuate) ligaments, which span the distance between available bony points and the intervening soft tissues:
Anatomy_Gray_602	Anatomy_Gray	Medial and lateral arcuate ligaments cross muscles of the posterior abdominal wall and attach to vertebrae, the transverse processes of vertebra LI and rib XII, respectively. A median arcuate ligament crosses the aorta and is continuous with the crus on each side. The posterior attachment of the diaphragm extends much farther inferiorly than the anterior attachment. Consequently, the diaphragm is an important component of the posterior abdominal wall, to which a number of viscera are related. The abdominal wall is continuous with the pelvic wall at the pelvic inlet, and the abdominal cavity is continuous with the pelvic cavity. The circular margin of the pelvic inlet is formed entirely by bone: posteriorly by the sacrum, anteriorly by the pubic symphysis, and laterally, on each side, by a distinct bony rim on the pelvic bone (Fig. 4.9).	Anatomy_Gray. Medial and lateral arcuate ligaments cross muscles of the posterior abdominal wall and attach to vertebrae, the transverse processes of vertebra LI and rib XII, respectively. A median arcuate ligament crosses the aorta and is continuous with the crus on each side. The posterior attachment of the diaphragm extends much farther inferiorly than the anterior attachment. Consequently, the diaphragm is an important component of the posterior abdominal wall, to which a number of viscera are related. The abdominal wall is continuous with the pelvic wall at the pelvic inlet, and the abdominal cavity is continuous with the pelvic cavity. The circular margin of the pelvic inlet is formed entirely by bone: posteriorly by the sacrum, anteriorly by the pubic symphysis, and laterally, on each side, by a distinct bony rim on the pelvic bone (Fig. 4.9).
Anatomy_Gray_603	Anatomy_Gray	Because of the way in which the sacrum and attached pelvic bones are angled posteriorly on the vertebral column, the pelvic cavity is not oriented in the same vertical plane as the abdominal cavity. Instead, the pelvic cavity projects posteriorly, and the inlet opens anteriorly and somewhat superiorly (Fig. 4.10). The abdomen is separated from the thorax by the diaphragm. Structures pass between the two regions through or posterior to the diaphragm (see Fig. 4.8). The pelvic inlet opens directly into the abdomen and structures pass between the abdomen and pelvis through it. The peritoneum lining the abdominal cavity is continuous with the peritoneum in the pelvis. Consequently, the abdominal cavity is entirely continuous with the pelvic cavity (Fig. 4.11). Infections in one region can therefore freely spread into the other.	Anatomy_Gray. Because of the way in which the sacrum and attached pelvic bones are angled posteriorly on the vertebral column, the pelvic cavity is not oriented in the same vertical plane as the abdominal cavity. Instead, the pelvic cavity projects posteriorly, and the inlet opens anteriorly and somewhat superiorly (Fig. 4.10). The abdomen is separated from the thorax by the diaphragm. Structures pass between the two regions through or posterior to the diaphragm (see Fig. 4.8). The pelvic inlet opens directly into the abdomen and structures pass between the abdomen and pelvis through it. The peritoneum lining the abdominal cavity is continuous with the peritoneum in the pelvis. Consequently, the abdominal cavity is entirely continuous with the pelvic cavity (Fig. 4.11). Infections in one region can therefore freely spread into the other.
Anatomy_Gray_604	Anatomy_Gray	The bladder expands superiorly from the pelvic cavity into the abdominal cavity and, during pregnancy, the uterus expands freely superiorly out of the pelvic cavity into the abdominal cavity. The abdomen communicates directly with the thigh through an aperture formed anteriorly between the inferior margin of the abdominal wall (marked by the inguinal ligament) and the pelvic bone (Fig. 4.12). Structures that pass through this aperture are: the major artery and vein of the lower limb; the femoral nerve, which innervates the quadriceps femoris muscle, which extends the knee; lymphatics; and the distal ends of psoas major and iliacus muscles, which flex the thigh at the hip joint. As vessels pass inferior to the inguinal ligament, their names change—the external iliac artery and vein of the abdomen become the femoral artery and vein of the thigh. Arrangement of abdominal viscera in the adult	Anatomy_Gray. The bladder expands superiorly from the pelvic cavity into the abdominal cavity and, during pregnancy, the uterus expands freely superiorly out of the pelvic cavity into the abdominal cavity. The abdomen communicates directly with the thigh through an aperture formed anteriorly between the inferior margin of the abdominal wall (marked by the inguinal ligament) and the pelvic bone (Fig. 4.12). Structures that pass through this aperture are: the major artery and vein of the lower limb; the femoral nerve, which innervates the quadriceps femoris muscle, which extends the knee; lymphatics; and the distal ends of psoas major and iliacus muscles, which flex the thigh at the hip joint. As vessels pass inferior to the inguinal ligament, their names change—the external iliac artery and vein of the abdomen become the femoral artery and vein of the thigh. Arrangement of abdominal viscera in the adult
Anatomy_Gray_605	Anatomy_Gray	Arrangement of abdominal viscera in the adult A basic knowledge of the development of the gastrointestinal tract is needed to understand the arrangement of viscera and mesenteries in the abdomen (Fig. 4.13). The early gastrointestinal tract is oriented longitudinally in the body cavity and is suspended from surrounding walls by a large dorsal mesentery and a much smaller ventral mesentery. Superiorly, the dorsal and ventral mesenteries are anchored to the diaphragm. The primitive gut tube consists of the foregut, the midgut, and the hindgut. Massive longitudinal growth of the gut tube, rotation of selected parts of the tube, and secondary fusion of some viscera and their associated mesenteries to the body wall participate in generating the adult arrangement of abdominal organs. Development of the foregut	Anatomy_Gray. Arrangement of abdominal viscera in the adult A basic knowledge of the development of the gastrointestinal tract is needed to understand the arrangement of viscera and mesenteries in the abdomen (Fig. 4.13). The early gastrointestinal tract is oriented longitudinally in the body cavity and is suspended from surrounding walls by a large dorsal mesentery and a much smaller ventral mesentery. Superiorly, the dorsal and ventral mesenteries are anchored to the diaphragm. The primitive gut tube consists of the foregut, the midgut, and the hindgut. Massive longitudinal growth of the gut tube, rotation of selected parts of the tube, and secondary fusion of some viscera and their associated mesenteries to the body wall participate in generating the adult arrangement of abdominal organs. Development of the foregut
Anatomy_Gray_606	Anatomy_Gray	Development of the foregut In abdominal regions, the foregut gives rise to the distal end of the esophagus, the stomach, and the proximal part of the duodenum. The foregut is the only part of the gut tube suspended from the wall by both the ventral and dorsal mesenteries. A diverticulum from the anterior aspect of the foregut grows into the ventral mesentery, giving rise to the liver and gallbladder, and, ultimately, to the ventral part of the pancreas. The dorsal part of the pancreas develops from an outgrowth of the foregut into the dorsal mesentery. The spleen develops in the dorsal mesentery in the region between the body wall and presumptive stomach. In the foregut, the developing stomach rotates clockwise and the associated dorsal mesentery, containing the spleen, moves to the left and greatly expands. During this process, part of the mesentery becomes associated with, and secondarily fuses with, the left side of the body wall.	Anatomy_Gray. Development of the foregut In abdominal regions, the foregut gives rise to the distal end of the esophagus, the stomach, and the proximal part of the duodenum. The foregut is the only part of the gut tube suspended from the wall by both the ventral and dorsal mesenteries. A diverticulum from the anterior aspect of the foregut grows into the ventral mesentery, giving rise to the liver and gallbladder, and, ultimately, to the ventral part of the pancreas. The dorsal part of the pancreas develops from an outgrowth of the foregut into the dorsal mesentery. The spleen develops in the dorsal mesentery in the region between the body wall and presumptive stomach. In the foregut, the developing stomach rotates clockwise and the associated dorsal mesentery, containing the spleen, moves to the left and greatly expands. During this process, part of the mesentery becomes associated with, and secondarily fuses with, the left side of the body wall.
Anatomy_Gray_607	Anatomy_Gray	At the same time, the duodenum, together with its dorsal mesentery and an appreciable part of the pancreas, swings to the right and fuses to the body wall. Secondary fusion of the duodenum to the body wall, massive growth of the liver in the ventral mesentery, and fusion of the superior surface of the liver to the diaphragm restrict the opening to the space enclosed by the ballooned dorsal mesentery associated with the stomach. This restricted opening is the omental foramen (epiploic foramen). The part of the abdominal cavity enclosed by the expanded dorsal mesentery, and posterior to the stomach, is the omental bursa (lesser sac). Access, through the omental foramen, to this space from the rest of the peritoneal cavity (greater sac) is inferior to the free edge of the ventral mesentery.	Anatomy_Gray. At the same time, the duodenum, together with its dorsal mesentery and an appreciable part of the pancreas, swings to the right and fuses to the body wall. Secondary fusion of the duodenum to the body wall, massive growth of the liver in the ventral mesentery, and fusion of the superior surface of the liver to the diaphragm restrict the opening to the space enclosed by the ballooned dorsal mesentery associated with the stomach. This restricted opening is the omental foramen (epiploic foramen). The part of the abdominal cavity enclosed by the expanded dorsal mesentery, and posterior to the stomach, is the omental bursa (lesser sac). Access, through the omental foramen, to this space from the rest of the peritoneal cavity (greater sac) is inferior to the free edge of the ventral mesentery.
Anatomy_Gray_608	Anatomy_Gray	Part of the dorsal mesentery that initially forms part of the lesser sac greatly enlarges in an inferior direction, and the two opposing surfaces of the mesentery fuse to form an apron-like structure (the greater omentum). The greater omentum is suspended from the greater curvature of the stomach, lies over other viscera in the abdominal cavity, and is the first structure observed when the abdominal cavity is opened anteriorly. Development of the midgut The midgut develops into the distal part of the duodenum and the jejunum, ileum, ascending colon, and proximal two-thirds of the transverse colon. A small yolk sac projects anteriorly from the developing midgut into the umbilicus.	Anatomy_Gray. Part of the dorsal mesentery that initially forms part of the lesser sac greatly enlarges in an inferior direction, and the two opposing surfaces of the mesentery fuse to form an apron-like structure (the greater omentum). The greater omentum is suspended from the greater curvature of the stomach, lies over other viscera in the abdominal cavity, and is the first structure observed when the abdominal cavity is opened anteriorly. Development of the midgut The midgut develops into the distal part of the duodenum and the jejunum, ileum, ascending colon, and proximal two-thirds of the transverse colon. A small yolk sac projects anteriorly from the developing midgut into the umbilicus.
Anatomy_Gray_609	Anatomy_Gray	Rapid growth of the gastrointestinal system results in a loop of the midgut herniating out of the abdominal cavity and into the umbilical cord. As the body grows in size and the connection with the yolk sac is lost, the midgut returns to the abdominal cavity. While this process is occurring, the two limbs of the midgut loop rotate counterclockwise around their combined central axis, and the part of the loop that becomes the cecum descends into the inferior right aspect of the cavity. The superior mesenteric artery, which supplies the midgut, is at the center of the axis of rotation. The cecum remains intraperitoneal, the ascending colon fuses with the body wall becoming secondarily retroperitoneal, and the transverse colon remains suspended by its dorsal mesentery (transverse mesocolon). The greater omentum hangs over the transverse colon and the mesocolon and usually fuses with these structures. Development of the hindgut	Anatomy_Gray. Rapid growth of the gastrointestinal system results in a loop of the midgut herniating out of the abdominal cavity and into the umbilical cord. As the body grows in size and the connection with the yolk sac is lost, the midgut returns to the abdominal cavity. While this process is occurring, the two limbs of the midgut loop rotate counterclockwise around their combined central axis, and the part of the loop that becomes the cecum descends into the inferior right aspect of the cavity. The superior mesenteric artery, which supplies the midgut, is at the center of the axis of rotation. The cecum remains intraperitoneal, the ascending colon fuses with the body wall becoming secondarily retroperitoneal, and the transverse colon remains suspended by its dorsal mesentery (transverse mesocolon). The greater omentum hangs over the transverse colon and the mesocolon and usually fuses with these structures. Development of the hindgut
Anatomy_Gray_610	Anatomy_Gray	Development of the hindgut The distal one-third of the transverse colon, descending colon, sigmoid colon, and superior part of the rectum develop from the hindgut. Proximal parts of the hindgut swing to the left and become the descending colon and sigmoid colon. The descending colon and its dorsal mesentery fuse to the body wall, while the sigmoid colon remains intraperitoneal. The sigmoid colon passes through the pelvic inlet and is continuous with the rectum at the level of vertebra SIII. Skin and muscles of the anterior The anterior rami of thoracic spinal nerves T7 to T12 follow the inferior slope of the lateral parts of the ribs and cross the costal margin to enter the abdominal wall (Fig. 4.14). Intercostal nerves T7 to T11 supply skin and muscle of the abdominal wall, as does the subcostal nerve T12. In addition, T5 and T6 supply upper parts of the external oblique muscle of the abdominal wall; T6 also supplies cutaneous innervation to skin over the xiphoid.	Anatomy_Gray. Development of the hindgut The distal one-third of the transverse colon, descending colon, sigmoid colon, and superior part of the rectum develop from the hindgut. Proximal parts of the hindgut swing to the left and become the descending colon and sigmoid colon. The descending colon and its dorsal mesentery fuse to the body wall, while the sigmoid colon remains intraperitoneal. The sigmoid colon passes through the pelvic inlet and is continuous with the rectum at the level of vertebra SIII. Skin and muscles of the anterior The anterior rami of thoracic spinal nerves T7 to T12 follow the inferior slope of the lateral parts of the ribs and cross the costal margin to enter the abdominal wall (Fig. 4.14). Intercostal nerves T7 to T11 supply skin and muscle of the abdominal wall, as does the subcostal nerve T12. In addition, T5 and T6 supply upper parts of the external oblique muscle of the abdominal wall; T6 also supplies cutaneous innervation to skin over the xiphoid.
Anatomy_Gray_611	Anatomy_Gray	T6 also supplies cutaneous innervation to skin over the xiphoid. Skin and muscle in the inguinal and suprapubic regions of the abdominal wall are innervated by L1 and not by thoracic nerves. Dermatomes of the anterior abdominal wall are indicated in Figure 4.14. In the midline, skin over the infrasternal angle is T6 and that around the umbilicus is T10. L1 innervates skin in the inguinal and suprapubic regions. Muscles of the abdominal wall are innervated segmentally in patterns that generally reflect the patterns of the overlying dermatomes. The groin is a weak area in the anterior abdominal wall During development, the gonads in both sexes descend from their sites of origin on the posterior abdominal wall into the pelvic cavity in women and the developing scrotum in men (Fig. 4.15).	Anatomy_Gray. T6 also supplies cutaneous innervation to skin over the xiphoid. Skin and muscle in the inguinal and suprapubic regions of the abdominal wall are innervated by L1 and not by thoracic nerves. Dermatomes of the anterior abdominal wall are indicated in Figure 4.14. In the midline, skin over the infrasternal angle is T6 and that around the umbilicus is T10. L1 innervates skin in the inguinal and suprapubic regions. Muscles of the abdominal wall are innervated segmentally in patterns that generally reflect the patterns of the overlying dermatomes. The groin is a weak area in the anterior abdominal wall During development, the gonads in both sexes descend from their sites of origin on the posterior abdominal wall into the pelvic cavity in women and the developing scrotum in men (Fig. 4.15).
Anatomy_Gray_612	Anatomy_Gray	During development, the gonads in both sexes descend from their sites of origin on the posterior abdominal wall into the pelvic cavity in women and the developing scrotum in men (Fig. 4.15). Before descent, a cord of tissue (the gubernaculum) passes through the anterior abdominal wall and connects the inferior pole of each gonad with primordia of the scrotum in men and the labia majora in women (labioscrotal swellings). A tubular extension (the processus vaginalis) of the peritoneal cavity and the accompanying muscular layers of the anterior abdominal wall project along the gubernaculum on each side into the labioscrotal swellings.	Anatomy_Gray. During development, the gonads in both sexes descend from their sites of origin on the posterior abdominal wall into the pelvic cavity in women and the developing scrotum in men (Fig. 4.15). Before descent, a cord of tissue (the gubernaculum) passes through the anterior abdominal wall and connects the inferior pole of each gonad with primordia of the scrotum in men and the labia majora in women (labioscrotal swellings). A tubular extension (the processus vaginalis) of the peritoneal cavity and the accompanying muscular layers of the anterior abdominal wall project along the gubernaculum on each side into the labioscrotal swellings.
Anatomy_Gray_613	Anatomy_Gray	In men, the testis, together with its neurovascular structures and its efferent duct (the ductus deferens) descends into the scrotum along a path, initially defined by the gubernaculum, between the processus vaginalis and the accompanying coverings derived from the abdominal wall. All that remains of the gubernaculum is a connective tissue remnant that attaches the caudal pole of the testis to the scrotum. The inguinal canal is the passage through the anterior abdominal wall created by the processus vaginalis. The spermatic cord is the tubular extension of the layers of the abdominal wall into the scrotum that contains all structures passing between the testis and the abdomen. The distal sac-like terminal end of the spermatic cord on each side contains the testis, associated structures, and the now isolated part of the peritoneal cavity (the cavity of the tunica vaginalis).	Anatomy_Gray. In men, the testis, together with its neurovascular structures and its efferent duct (the ductus deferens) descends into the scrotum along a path, initially defined by the gubernaculum, between the processus vaginalis and the accompanying coverings derived from the abdominal wall. All that remains of the gubernaculum is a connective tissue remnant that attaches the caudal pole of the testis to the scrotum. The inguinal canal is the passage through the anterior abdominal wall created by the processus vaginalis. The spermatic cord is the tubular extension of the layers of the abdominal wall into the scrotum that contains all structures passing between the testis and the abdomen. The distal sac-like terminal end of the spermatic cord on each side contains the testis, associated structures, and the now isolated part of the peritoneal cavity (the cavity of the tunica vaginalis).
Anatomy_Gray_614	Anatomy_Gray	In women, the gonads descend to a position just inside the pelvic cavity and never pass through the anterior abdominal wall. As a result, the only major structure passing through the inguinal canal is a derivative of the gubernaculum (the round ligament of the uterus). In both men and women, the groin (inguinal region) is a weak area in the abdominal wall (Fig. 4.15) and is the site of inguinal hernias.	Anatomy_Gray. In women, the gonads descend to a position just inside the pelvic cavity and never pass through the anterior abdominal wall. As a result, the only major structure passing through the inguinal canal is a derivative of the gubernaculum (the round ligament of the uterus). In both men and women, the groin (inguinal region) is a weak area in the abdominal wall (Fig. 4.15) and is the site of inguinal hernias.
Anatomy_Gray_615	Anatomy_Gray	The transpyloric plane is a horizontal plane that transects the body through the lower aspect of vertebra LI (Fig. 4.16). It: is about midway between the jugular notch and the pubic symphysis, and crosses the costal margin on each side at roughly the ninth costal cartilage; crosses through the opening of the stomach into the duodenum (the pyloric orifice), which is just to the right of the body of LI; the duodenum then makes a characteristic C-shaped loop on the posterior abdominal wall and crosses the midline to open into the jejunum just to the left of the body of vertebra LII, whereas the head of the pancreas is enclosed by the loop of the duodenum, and the body of the pancreas extends across the midline to the left; crosses through the body of the pancreas; and approximates the position of the hila of the kidneys; though because the left kidney is slightly higher than the right, the transpyloric plane crosses through the inferior aspect of the left hilum and the superior part of	Anatomy_Gray. The transpyloric plane is a horizontal plane that transects the body through the lower aspect of vertebra LI (Fig. 4.16). It: is about midway between the jugular notch and the pubic symphysis, and crosses the costal margin on each side at roughly the ninth costal cartilage; crosses through the opening of the stomach into the duodenum (the pyloric orifice), which is just to the right of the body of LI; the duodenum then makes a characteristic C-shaped loop on the posterior abdominal wall and crosses the midline to open into the jejunum just to the left of the body of vertebra LII, whereas the head of the pancreas is enclosed by the loop of the duodenum, and the body of the pancreas extends across the midline to the left; crosses through the body of the pancreas; and approximates the position of the hila of the kidneys; though because the left kidney is slightly higher than the right, the transpyloric plane crosses through the inferior aspect of the left hilum and the superior part of
Anatomy_Gray_616	Anatomy_Gray	of the hila of the kidneys; though because the left kidney is slightly higher than the right, the transpyloric plane crosses through the inferior aspect of the left hilum and the superior part of the right hilum.	Anatomy_Gray. of the hila of the kidneys; though because the left kidney is slightly higher than the right, the transpyloric plane crosses through the inferior aspect of the left hilum and the superior part of the right hilum.
Anatomy_Gray_617	Anatomy_Gray	The gastrointestinal system and its derivatives are supplied by three major arteries	Anatomy_Gray. The gastrointestinal system and its derivatives are supplied by three major arteries
Anatomy_Gray_618	Anatomy_Gray	Three large unpaired arteries branch from the anterior surface of the abdominal aorta to supply the abdominal part of the gastrointestinal tract and all of the structures (liver, pancreas, and gallbladder) to which this part of the gut gives rise during development (Fig. 4.17). These arteries pass through derivatives of the dorsal and ventral mesenteries to reach the target viscera. These vessels therefore also supply structures such as the spleen and lymph nodes that develop in the mesenteries. These three arteries are: the celiac artery, which branches from the abdominal aorta at the upper border of vertebra LI and supplies the foregut; the superior mesenteric artery, which arises from the abdominal aorta at the lower border of vertebra LI and supplies the midgut; and the inferior mesenteric artery, which branches from the abdominal aorta at approximately vertebral level LIII and supplies the hindgut. Venous shunts from left to right	Anatomy_Gray. Three large unpaired arteries branch from the anterior surface of the abdominal aorta to supply the abdominal part of the gastrointestinal tract and all of the structures (liver, pancreas, and gallbladder) to which this part of the gut gives rise during development (Fig. 4.17). These arteries pass through derivatives of the dorsal and ventral mesenteries to reach the target viscera. These vessels therefore also supply structures such as the spleen and lymph nodes that develop in the mesenteries. These three arteries are: the celiac artery, which branches from the abdominal aorta at the upper border of vertebra LI and supplies the foregut; the superior mesenteric artery, which arises from the abdominal aorta at the lower border of vertebra LI and supplies the midgut; and the inferior mesenteric artery, which branches from the abdominal aorta at approximately vertebral level LIII and supplies the hindgut. Venous shunts from left to right
Anatomy_Gray_619	Anatomy_Gray	Venous shunts from left to right All blood returning to the heart from regions of the body other than the lungs flows into the right atrium of the heart. The inferior vena cava is the major systemic vein in the abdomen and drains this region together with the pelvis, perineum, and both lower limbs (Fig. 4.18). The inferior vena cava lies to the right of the vertebral column and penetrates the central tendon of the diaphragm at approximately vertebral level TVIII. A number of large vessels cross the midline to deliver blood from the left side of the body to the inferior vena cava. One of the most significant is the left renal vein, which drains the kidney, suprarenal gland, and gonad on the same side. Another is the left common iliac vein, which crosses the midline at approximately vertebral level LV to join with its partner on the right to form the inferior vena cava. These veins drain the lower limbs, the pelvis, the perineum, and parts of the abdominal wall.	Anatomy_Gray. Venous shunts from left to right All blood returning to the heart from regions of the body other than the lungs flows into the right atrium of the heart. The inferior vena cava is the major systemic vein in the abdomen and drains this region together with the pelvis, perineum, and both lower limbs (Fig. 4.18). The inferior vena cava lies to the right of the vertebral column and penetrates the central tendon of the diaphragm at approximately vertebral level TVIII. A number of large vessels cross the midline to deliver blood from the left side of the body to the inferior vena cava. One of the most significant is the left renal vein, which drains the kidney, suprarenal gland, and gonad on the same side. Another is the left common iliac vein, which crosses the midline at approximately vertebral level LV to join with its partner on the right to form the inferior vena cava. These veins drain the lower limbs, the pelvis, the perineum, and parts of the abdominal wall.
Anatomy_Gray_620	Anatomy_Gray	Other vessels crossing the midline include the left lumbar veins, which drain the back and posterior abdominal wall on the left side. All venous drainage from the through the liver Blood from abdominal parts of the gastrointestinal system and the spleen passes through a second vascular bed, in the liver, before ultimately returning to the heart (Fig. 4.19). Venous blood from the digestive tract, pancreas, gallbladder, and spleen enters the inferior surface of the liver through the large hepatic portal vein. This vein then ramifies like an artery to distribute blood to small endothelial-lined hepatic sinusoids, which form the vascular exchange network of the liver. After passing through the sinusoids, the blood collects in a number of short hepatic veins, which drain into the inferior vena cava just before the inferior vena cava penetrates the diaphragm and enters the right atrium of the heart.	Anatomy_Gray. Other vessels crossing the midline include the left lumbar veins, which drain the back and posterior abdominal wall on the left side. All venous drainage from the through the liver Blood from abdominal parts of the gastrointestinal system and the spleen passes through a second vascular bed, in the liver, before ultimately returning to the heart (Fig. 4.19). Venous blood from the digestive tract, pancreas, gallbladder, and spleen enters the inferior surface of the liver through the large hepatic portal vein. This vein then ramifies like an artery to distribute blood to small endothelial-lined hepatic sinusoids, which form the vascular exchange network of the liver. After passing through the sinusoids, the blood collects in a number of short hepatic veins, which drain into the inferior vena cava just before the inferior vena cava penetrates the diaphragm and enters the right atrium of the heart.
Anatomy_Gray_621	Anatomy_Gray	Normally, vascular beds drained by the hepatic portal system interconnect, through small veins, with beds drained by systemic vessels, which ultimately connect directly with either the superior or inferior vena cava. Among the clinically most important regions of overlap between the portal and caval systems are those at each end of the abdominal part of the gastrointestinal system: around the inferior end of the esophagus; around the inferior part of the rectum. Small veins that accompany the degenerate umbilical vein (round ligament of the liver) establish another important portacaval anastomosis. The round ligament of the liver connects the umbilicus of the anterior abdominal wall with the left branch of the portal vein as it enters the liver. The small veins that accompany this ligament form a connection between the portal system and para-umbilical regions of the abdominal wall, which drain into systemic veins.	Anatomy_Gray. Normally, vascular beds drained by the hepatic portal system interconnect, through small veins, with beds drained by systemic vessels, which ultimately connect directly with either the superior or inferior vena cava. Among the clinically most important regions of overlap between the portal and caval systems are those at each end of the abdominal part of the gastrointestinal system: around the inferior end of the esophagus; around the inferior part of the rectum. Small veins that accompany the degenerate umbilical vein (round ligament of the liver) establish another important portacaval anastomosis. The round ligament of the liver connects the umbilicus of the anterior abdominal wall with the left branch of the portal vein as it enters the liver. The small veins that accompany this ligament form a connection between the portal system and para-umbilical regions of the abdominal wall, which drain into systemic veins.
Anatomy_Gray_622	Anatomy_Gray	Other regions where portal and caval systems interconnect include: where the liver is in direct contact with the diaphragm (the bare area of the liver); where the wall of the gastrointestinal tract is in direct contact with the posterior abdominal wall (retroperitoneal areas of the large and small intestine); and the posterior surface of the pancreas (much of the pancreas is secondarily retroperitoneal). Blockage of the hepatic portal vein or of vascular channels in the liver	Anatomy_Gray. Other regions where portal and caval systems interconnect include: where the liver is in direct contact with the diaphragm (the bare area of the liver); where the wall of the gastrointestinal tract is in direct contact with the posterior abdominal wall (retroperitoneal areas of the large and small intestine); and the posterior surface of the pancreas (much of the pancreas is secondarily retroperitoneal). Blockage of the hepatic portal vein or of vascular channels in the liver
Anatomy_Gray_623	Anatomy_Gray	Blockage of the hepatic portal vein or of vascular channels in the liver Blockage of the hepatic portal vein or of vascular channels in the liver can affect the pattern of venous return from abdominal parts of the gastrointestinal system. Vessels that interconnect the portal and caval systems can become greatly enlarged and tortuous, allowing blood in tributaries of the portal system to bypass the liver, enter the caval system, and thereby return to the heart. Portal hypertension can result in esophageal and rectal varices and in caput medusae in which systemic vessels that radiate from para-umbilical veins enlarge and become visible on the abdominal wall. Abdominal viscera are supplied by a large prevertebral plexus Innervation of the abdominal viscera is derived from a large prevertebral plexus associated mainly with the anterior and lateral surfaces of the aorta (Fig. 4.20). Branches are distributed to target tissues along vessels that originate from the abdominal aorta.	Anatomy_Gray. Blockage of the hepatic portal vein or of vascular channels in the liver Blockage of the hepatic portal vein or of vascular channels in the liver can affect the pattern of venous return from abdominal parts of the gastrointestinal system. Vessels that interconnect the portal and caval systems can become greatly enlarged and tortuous, allowing blood in tributaries of the portal system to bypass the liver, enter the caval system, and thereby return to the heart. Portal hypertension can result in esophageal and rectal varices and in caput medusae in which systemic vessels that radiate from para-umbilical veins enlarge and become visible on the abdominal wall. Abdominal viscera are supplied by a large prevertebral plexus Innervation of the abdominal viscera is derived from a large prevertebral plexus associated mainly with the anterior and lateral surfaces of the aorta (Fig. 4.20). Branches are distributed to target tissues along vessels that originate from the abdominal aorta.
Anatomy_Gray_624	Anatomy_Gray	The prevertebral plexus contains sympathetic, parasympathetic, and visceral sensory components: Sympathetic components originate from spinal cord levels T5 to L2. Parasympathetic components are from the vagus nerve [X] and spinal cord levels S2 to S4. Visceral sensory fibers generally parallel the motor pathways. The abdomen is the part of the trunk inferior to the thorax (Fig. 4.21). Its musculomembranous walls surround a large cavity (the abdominal cavity), which is bounded superiorly by the diaphragm and inferiorly by the pelvic inlet. The abdominal cavity may extend superiorly as high as the fourth intercostal space, and is continuous inferiorly with the pelvic cavity. It contains the peritoneal cavity and the abdominal viscera. Topographical divisions of the abdomen are used to describe the location of abdominal organs and the pain associated with abdominal problems. The two schemes most often used are: a four-quadrant pattern and a nine-region pattern.	Anatomy_Gray. The prevertebral plexus contains sympathetic, parasympathetic, and visceral sensory components: Sympathetic components originate from spinal cord levels T5 to L2. Parasympathetic components are from the vagus nerve [X] and spinal cord levels S2 to S4. Visceral sensory fibers generally parallel the motor pathways. The abdomen is the part of the trunk inferior to the thorax (Fig. 4.21). Its musculomembranous walls surround a large cavity (the abdominal cavity), which is bounded superiorly by the diaphragm and inferiorly by the pelvic inlet. The abdominal cavity may extend superiorly as high as the fourth intercostal space, and is continuous inferiorly with the pelvic cavity. It contains the peritoneal cavity and the abdominal viscera. Topographical divisions of the abdomen are used to describe the location of abdominal organs and the pain associated with abdominal problems. The two schemes most often used are: a four-quadrant pattern and a nine-region pattern.
Anatomy_Gray_625	Anatomy_Gray	A horizontal transumbilical plane passing through the umbilicus and the intervertebral disc between vertebrae LIII and LIV and intersecting with the vertical median plane divides the abdomen into four quadrants—the right upper, left upper, right lower, and left lower quadrants (Fig. 4.22). The nine-region pattern is based on two horizontal and two vertical planes (Fig. 4.23). The superior horizontal plane (the subcostal plane) is immediately inferior to the costal margins, which places it at the lower border of the costal cartilage of rib X and passing posteriorly through the body of vertebra LIII. (Note, however, that sometimes the transpyloric plane, halfway between the jugular notch and the symphysis pubis or halfway between the umbilicus and the inferior end of the body of the sternum, passing posteriorly through the lower border of vertebra LI and intersecting with the costal margin at the ends of the ninth costal cartilages, is used instead.)	Anatomy_Gray. A horizontal transumbilical plane passing through the umbilicus and the intervertebral disc between vertebrae LIII and LIV and intersecting with the vertical median plane divides the abdomen into four quadrants—the right upper, left upper, right lower, and left lower quadrants (Fig. 4.22). The nine-region pattern is based on two horizontal and two vertical planes (Fig. 4.23). The superior horizontal plane (the subcostal plane) is immediately inferior to the costal margins, which places it at the lower border of the costal cartilage of rib X and passing posteriorly through the body of vertebra LIII. (Note, however, that sometimes the transpyloric plane, halfway between the jugular notch and the symphysis pubis or halfway between the umbilicus and the inferior end of the body of the sternum, passing posteriorly through the lower border of vertebra LI and intersecting with the costal margin at the ends of the ninth costal cartilages, is used instead.)
Anatomy_Gray_626	Anatomy_Gray	The inferior horizontal plane (the intertubercular plane) connects the tubercles of the iliac crests, which are palpable structures 5 cm posterior to the anterior superior iliac spines, and passes through the upper part of the body of vertebra LV. The vertical planes pass from the midpoint of the clavicles inferiorly to a point midway between the anterior superior iliac spine and pubic symphysis. These four planes establish the topographical divisions in the nine-region organization. The following designations are used for each region: superiorly the right hypochondrium, the epigastric region, and the left hypochondrium; inferiorly the right groin (inguinal region), pubic region, and left groin (inguinal region); and in the middle the right flank (lateral region), the umbilical region, and the left flank (lateral region) (Fig. 4.23).	Anatomy_Gray. The inferior horizontal plane (the intertubercular plane) connects the tubercles of the iliac crests, which are palpable structures 5 cm posterior to the anterior superior iliac spines, and passes through the upper part of the body of vertebra LV. The vertical planes pass from the midpoint of the clavicles inferiorly to a point midway between the anterior superior iliac spine and pubic symphysis. These four planes establish the topographical divisions in the nine-region organization. The following designations are used for each region: superiorly the right hypochondrium, the epigastric region, and the left hypochondrium; inferiorly the right groin (inguinal region), pubic region, and left groin (inguinal region); and in the middle the right flank (lateral region), the umbilical region, and the left flank (lateral region) (Fig. 4.23).
Anatomy_Gray_627	Anatomy_Gray	The abdominal wall covers a large area. It is bounded superiorly by the xiphoid process and costal margins, posteriorly by the vertebral column, and inferiorly by the upper parts of the pelvic bones. Its layers consist of skin, superficial fascia (subcutaneous tissue), muscles and their associated deep fascias, extraperitoneal fascia, and parietal peritoneum (Fig. 4.24). The superficial fascia of the abdominal wall (subcutaneous tissue of abdomen) is a layer of fatty connective tissue. It is usually a single layer similar to, and continuous with, the superficial fascia throughout other regions of the body. However, in the lower region of the anterior part of the abdominal wall, below the umbilicus, it forms two layers: a superficial fatty layer and a deeper membranous layer.	Anatomy_Gray. The abdominal wall covers a large area. It is bounded superiorly by the xiphoid process and costal margins, posteriorly by the vertebral column, and inferiorly by the upper parts of the pelvic bones. Its layers consist of skin, superficial fascia (subcutaneous tissue), muscles and their associated deep fascias, extraperitoneal fascia, and parietal peritoneum (Fig. 4.24). The superficial fascia of the abdominal wall (subcutaneous tissue of abdomen) is a layer of fatty connective tissue. It is usually a single layer similar to, and continuous with, the superficial fascia throughout other regions of the body. However, in the lower region of the anterior part of the abdominal wall, below the umbilicus, it forms two layers: a superficial fatty layer and a deeper membranous layer.
Anatomy_Gray_628	Anatomy_Gray	The superficial fatty layer of superficial fascia (Camper’s fascia) contains fat and varies in thickness (Figs. 4.25 and 4.26). It is continuous over the inguinal ligament with the superficial fascia of the thigh and with a similar layer in the perineum. In men, this superficial layer continues over the penis and, after losing its fat and fusing with the deeper layer of superficial fascia, continues into the scrotum where it forms a specialized fascial layer containing smooth muscle fibers (the dartos fascia). In women, this superficial layer retains some fat and is a component of the labia majora.	Anatomy_Gray. The superficial fatty layer of superficial fascia (Camper’s fascia) contains fat and varies in thickness (Figs. 4.25 and 4.26). It is continuous over the inguinal ligament with the superficial fascia of the thigh and with a similar layer in the perineum. In men, this superficial layer continues over the penis and, after losing its fat and fusing with the deeper layer of superficial fascia, continues into the scrotum where it forms a specialized fascial layer containing smooth muscle fibers (the dartos fascia). In women, this superficial layer retains some fat and is a component of the labia majora.
Anatomy_Gray_629	Anatomy_Gray	The deeper membranous layer of superficial fascia (Scarpa’s fascia) is thin and membranous, and contains little or no fat (Fig. 4.25). Inferiorly, it continues into the thigh, but just below the inguinal ligament, it fuses with the deep fascia of the thigh (the fascia lata; Fig. 4.26). In the midline, it is firmly attached to the linea alba and the symphysis pubis. It continues into the anterior part of the perineum where it is firmly attached to the ischiopubic rami and to the posterior margin of the perineal membrane. Here, it is referred to as the superficial perineal fascia (Colles’ fascia).	Anatomy_Gray. The deeper membranous layer of superficial fascia (Scarpa’s fascia) is thin and membranous, and contains little or no fat (Fig. 4.25). Inferiorly, it continues into the thigh, but just below the inguinal ligament, it fuses with the deep fascia of the thigh (the fascia lata; Fig. 4.26). In the midline, it is firmly attached to the linea alba and the symphysis pubis. It continues into the anterior part of the perineum where it is firmly attached to the ischiopubic rami and to the posterior margin of the perineal membrane. Here, it is referred to as the superficial perineal fascia (Colles’ fascia).
Anatomy_Gray_630	Anatomy_Gray	In men, the deeper membranous layer of superficial fascia blends with the superficial layer as they both pass over the penis, forming the superficial fascia of the penis, before they continue into the scrotum where they form the dartos fascia (Fig. 4.25). Also in men, extensions of the deeper membranous layer of superficial fascia attached to the pubic symphysis pass inferiorly onto the dorsum and sides of the penis to form the fundiform ligament of penis. In women, the membranous layer of the superficial fascia continues into the labia majora and the anterior part of the perineum.	Anatomy_Gray. In men, the deeper membranous layer of superficial fascia blends with the superficial layer as they both pass over the penis, forming the superficial fascia of the penis, before they continue into the scrotum where they form the dartos fascia (Fig. 4.25). Also in men, extensions of the deeper membranous layer of superficial fascia attached to the pubic symphysis pass inferiorly onto the dorsum and sides of the penis to form the fundiform ligament of penis. In women, the membranous layer of the superficial fascia continues into the labia majora and the anterior part of the perineum.
Anatomy_Gray_631	Anatomy_Gray	There are five muscles in the anterolateral group of abdominal wall muscles: three flat muscles whose fibers begin posterolaterally, pass anteriorly, and are replaced by an aponeurosis as the muscle continues toward the midline—the external oblique, internal oblique, and transversus abdominis muscles; two vertical muscles, near the midline, which are enclosed within a tendinous sheath formed by the aponeuroses of the flat muscles—the rectus abdominis and pyramidalis muscles. Each of these five muscles has specific actions, but together the muscles are critical for the maintenance of many normal physiological functions. By their positioning, they form a firm, but flexible, wall that keeps the abdominal viscera within the abdominal cavity, protects the viscera from injury, and helps maintain the position of the viscera in the erect posture against the action of gravity.	Anatomy_Gray. There are five muscles in the anterolateral group of abdominal wall muscles: three flat muscles whose fibers begin posterolaterally, pass anteriorly, and are replaced by an aponeurosis as the muscle continues toward the midline—the external oblique, internal oblique, and transversus abdominis muscles; two vertical muscles, near the midline, which are enclosed within a tendinous sheath formed by the aponeuroses of the flat muscles—the rectus abdominis and pyramidalis muscles. Each of these five muscles has specific actions, but together the muscles are critical for the maintenance of many normal physiological functions. By their positioning, they form a firm, but flexible, wall that keeps the abdominal viscera within the abdominal cavity, protects the viscera from injury, and helps maintain the position of the viscera in the erect posture against the action of gravity.
Anatomy_Gray_632	Anatomy_Gray	In addition, contraction of these muscles assists in both quiet and forced expiration by pushing the viscera upward (which helps push the relaxed diaphragm further into the thoracic cavity) and in coughing and vomiting. All these muscles are also involved in any action that increases intraabdominal pressure, including parturition (childbirth), micturition (urination), and defecation (expulsion of feces from the rectum). The most superficial of the three flat muscles in the anterolateral group of abdominal wall muscles is the external oblique, which is immediately deep to the superficial fascia (Fig. 4.27, Table 4.1). Its laterally placed muscle fibers pass in an inferomedial direction, while its large aponeurotic component covers the anterior part of the abdominal wall to the midline. Approaching the midline, the aponeuroses are entwined, forming the linea alba, which extends from the xiphoid process to the pubic symphysis.	Anatomy_Gray. In addition, contraction of these muscles assists in both quiet and forced expiration by pushing the viscera upward (which helps push the relaxed diaphragm further into the thoracic cavity) and in coughing and vomiting. All these muscles are also involved in any action that increases intraabdominal pressure, including parturition (childbirth), micturition (urination), and defecation (expulsion of feces from the rectum). The most superficial of the three flat muscles in the anterolateral group of abdominal wall muscles is the external oblique, which is immediately deep to the superficial fascia (Fig. 4.27, Table 4.1). Its laterally placed muscle fibers pass in an inferomedial direction, while its large aponeurotic component covers the anterior part of the abdominal wall to the midline. Approaching the midline, the aponeuroses are entwined, forming the linea alba, which extends from the xiphoid process to the pubic symphysis.
Anatomy_Gray_633	Anatomy_Gray	The lower border of the external oblique aponeurosis forms the inguinal ligament on each side (Fig. 4.27). This thickened reinforced free edge of the external oblique aponeurosis passes between the anterior superior iliac spine laterally and the pubic tubercle medially (Fig. 4.28). It folds under itself forming a trough, which plays an important role in the formation of the inguinal canal. Several other ligaments are also formed from extensions of the fibers at the medial end of the inguinal ligament: The lacunar ligament is a crescent-shaped extension of fibers at the medial end of the inguinal ligament that pass backward to attach to the pecten pubis on the superior ramus of the pubic bone (Figs. 4.28 and 4.29). Additional fibers extend from the lacunar ligament along the pecten pubis of the pelvic brim to form the pectineal (Cooper’s) ligament.	Anatomy_Gray. The lower border of the external oblique aponeurosis forms the inguinal ligament on each side (Fig. 4.27). This thickened reinforced free edge of the external oblique aponeurosis passes between the anterior superior iliac spine laterally and the pubic tubercle medially (Fig. 4.28). It folds under itself forming a trough, which plays an important role in the formation of the inguinal canal. Several other ligaments are also formed from extensions of the fibers at the medial end of the inguinal ligament: The lacunar ligament is a crescent-shaped extension of fibers at the medial end of the inguinal ligament that pass backward to attach to the pecten pubis on the superior ramus of the pubic bone (Figs. 4.28 and 4.29). Additional fibers extend from the lacunar ligament along the pecten pubis of the pelvic brim to form the pectineal (Cooper’s) ligament.
Anatomy_Gray_634	Anatomy_Gray	Additional fibers extend from the lacunar ligament along the pecten pubis of the pelvic brim to form the pectineal (Cooper’s) ligament. Deep to the external oblique muscle is the internal oblique muscle, which is the second of the three flat muscles (Fig. 4.30, Table 4.1). This muscle is smaller and thinner than the external oblique, with most of its muscle fibers passing in a superomedial direction. Its lateral muscular components end anteriorly as an aponeurosis that blends into the linea alba at the midline. Deep to the internal oblique muscle is the transversus abdominis muscle (Fig. 4.31, Table 4.1), so named because of the direction of most of its muscle fibers. It ends in an anterior aponeurosis, which blends with the linea alba at the midline.	Anatomy_Gray. Additional fibers extend from the lacunar ligament along the pecten pubis of the pelvic brim to form the pectineal (Cooper’s) ligament. Deep to the external oblique muscle is the internal oblique muscle, which is the second of the three flat muscles (Fig. 4.30, Table 4.1). This muscle is smaller and thinner than the external oblique, with most of its muscle fibers passing in a superomedial direction. Its lateral muscular components end anteriorly as an aponeurosis that blends into the linea alba at the midline. Deep to the internal oblique muscle is the transversus abdominis muscle (Fig. 4.31, Table 4.1), so named because of the direction of most of its muscle fibers. It ends in an anterior aponeurosis, which blends with the linea alba at the midline.
Anatomy_Gray_635	Anatomy_Gray	Each of the three flat muscles is covered on its anterior and posterior surfaces by a layer of deep (or investing) fascia. In general, these layers are unremarkable except for the layer deep to the transversus abdominis muscle (the transversalis fascia), which is better developed. The transversalis fascia is a continuous layer of deep fascia that lines the abdominal cavity and continues into the pelvic cavity. It crosses the midline anteriorly, associating with the transversalis fascia of the opposite side, and is continuous with the fascia on the inferior surface of the diaphragm. It is continuous posteriorly with the deep fascia covering the muscles of the posterior abdominal wall and attaches to the thoracolumbar fascia.	Anatomy_Gray. Each of the three flat muscles is covered on its anterior and posterior surfaces by a layer of deep (or investing) fascia. In general, these layers are unremarkable except for the layer deep to the transversus abdominis muscle (the transversalis fascia), which is better developed. The transversalis fascia is a continuous layer of deep fascia that lines the abdominal cavity and continues into the pelvic cavity. It crosses the midline anteriorly, associating with the transversalis fascia of the opposite side, and is continuous with the fascia on the inferior surface of the diaphragm. It is continuous posteriorly with the deep fascia covering the muscles of the posterior abdominal wall and attaches to the thoracolumbar fascia.
Anatomy_Gray_636	Anatomy_Gray	After attaching to the crest of the ilium, the transversalis fascia blends with the fascia covering the muscles associated with the upper regions of the pelvic bones and with similar fascia covering the muscles of the pelvic cavity. At this point, it is referred to as the parietal pelvic (or endopelvic) fascia. There is therefore a continuous layer of deep fascia surrounding the abdominal cavity that is thick in some areas, thin in others, attached or free, and participates in the formation of specialized structures. The two vertical muscles in the anterolateral group of abdominal wall muscles are the large rectus abdominis and the small pyramidalis (Fig. 4.32, Table 4.1).	Anatomy_Gray. After attaching to the crest of the ilium, the transversalis fascia blends with the fascia covering the muscles associated with the upper regions of the pelvic bones and with similar fascia covering the muscles of the pelvic cavity. At this point, it is referred to as the parietal pelvic (or endopelvic) fascia. There is therefore a continuous layer of deep fascia surrounding the abdominal cavity that is thick in some areas, thin in others, attached or free, and participates in the formation of specialized structures. The two vertical muscles in the anterolateral group of abdominal wall muscles are the large rectus abdominis and the small pyramidalis (Fig. 4.32, Table 4.1).
Anatomy_Gray_637	Anatomy_Gray	The two vertical muscles in the anterolateral group of abdominal wall muscles are the large rectus abdominis and the small pyramidalis (Fig. 4.32, Table 4.1). The rectus abdominis is a long, flat muscle and extends the length of the anterior abdominal wall. It is a paired muscle, separated in the midline by the linea alba, and it widens and thins as it ascends from the pubic symphysis to the costal margin. Along its course, it is intersected by three or four transverse fibrous bands or tendinous intersections (Fig. 4.32). These are easily visible on individuals with well-developed rectus abdominis muscles. The second vertical muscle is the pyramidalis. This small, triangular muscle, which may be absent, is anterior to the rectus abdominis and has its base on the pubis, and its apex is attached superiorly and medially to the linea alba (Fig. 4.32).	Anatomy_Gray. The two vertical muscles in the anterolateral group of abdominal wall muscles are the large rectus abdominis and the small pyramidalis (Fig. 4.32, Table 4.1). The rectus abdominis is a long, flat muscle and extends the length of the anterior abdominal wall. It is a paired muscle, separated in the midline by the linea alba, and it widens and thins as it ascends from the pubic symphysis to the costal margin. Along its course, it is intersected by three or four transverse fibrous bands or tendinous intersections (Fig. 4.32). These are easily visible on individuals with well-developed rectus abdominis muscles. The second vertical muscle is the pyramidalis. This small, triangular muscle, which may be absent, is anterior to the rectus abdominis and has its base on the pubis, and its apex is attached superiorly and medially to the linea alba (Fig. 4.32).
Anatomy_Gray_638	Anatomy_Gray	The rectus abdominis and pyramidalis muscles are enclosed in an aponeurotic tendinous sheath (the rectus sheath) formed by a unique layering of the aponeuroses of the external and internal oblique, and transversus abdominis muscles (Fig. 4.33). The rectus sheath completely encloses the upper three-quarters of the rectus abdominis and covers the anterior surface of the lower one-quarter of the muscle. As no sheath covers the posterior surface of the lower quarter of the rectus abdominis muscle, the muscle at this point is in direct contact with the transversalis fascia. The formation of the rectus sheath surrounding the upper three-quarters of the rectus abdominis muscle has the following pattern: The anterior wall consists of the aponeurosis of the external oblique and half of the aponeurosis of the internal oblique, which splits at the lateral margin of the rectus abdominis.	Anatomy_Gray. The rectus abdominis and pyramidalis muscles are enclosed in an aponeurotic tendinous sheath (the rectus sheath) formed by a unique layering of the aponeuroses of the external and internal oblique, and transversus abdominis muscles (Fig. 4.33). The rectus sheath completely encloses the upper three-quarters of the rectus abdominis and covers the anterior surface of the lower one-quarter of the muscle. As no sheath covers the posterior surface of the lower quarter of the rectus abdominis muscle, the muscle at this point is in direct contact with the transversalis fascia. The formation of the rectus sheath surrounding the upper three-quarters of the rectus abdominis muscle has the following pattern: The anterior wall consists of the aponeurosis of the external oblique and half of the aponeurosis of the internal oblique, which splits at the lateral margin of the rectus abdominis.
Anatomy_Gray_639	Anatomy_Gray	The anterior wall consists of the aponeurosis of the external oblique and half of the aponeurosis of the internal oblique, which splits at the lateral margin of the rectus abdominis. The posterior wall of the rectus sheath consists of the other half of the aponeurosis of the internal oblique and the aponeurosis of the transversus abdominis. At a point midway between the umbilicus and the pubic symphysis, corresponding to the beginning of the lower one-quarter of the rectus abdominis muscle, all of the aponeuroses move anterior to the rectus muscle. There is no posterior wall of the rectus sheath and the anterior wall of the sheath consists of the aponeuroses of the external oblique, the internal oblique, and the transversus abdominis muscles. From this point inferiorly, the rectus abdominis muscle is in direct contact with the transversalis fascia. Marking this point of transition is an arch of fibers (the arcuate line; see Fig. 4.32).	Anatomy_Gray. The anterior wall consists of the aponeurosis of the external oblique and half of the aponeurosis of the internal oblique, which splits at the lateral margin of the rectus abdominis. The posterior wall of the rectus sheath consists of the other half of the aponeurosis of the internal oblique and the aponeurosis of the transversus abdominis. At a point midway between the umbilicus and the pubic symphysis, corresponding to the beginning of the lower one-quarter of the rectus abdominis muscle, all of the aponeuroses move anterior to the rectus muscle. There is no posterior wall of the rectus sheath and the anterior wall of the sheath consists of the aponeuroses of the external oblique, the internal oblique, and the transversus abdominis muscles. From this point inferiorly, the rectus abdominis muscle is in direct contact with the transversalis fascia. Marking this point of transition is an arch of fibers (the arcuate line; see Fig. 4.32).