Superior vena cava syndrome pathophysiology: Difference between revisions
No edit summary |
|||
| Line 6: | Line 6: | ||
[[Superior vena cava]] ([[SVC]]) syndrome arises from the obstruction of venous blood drainage of the superior vena cava, which is normally is involved in the major blood flow return from [[head]], [[neck]], upper extremities, and upper thorax to the [[heart]]. Superior vena cava syndrome is a complication from a partial or complete obstruction due to malignant causes (60%) or benign causes (20%). This syndrome may be caused by the invasion of the venous wall associated with intravascular thrombosis, enlarged nodes, enlarged [[ascending aorta]], or more simply, by extrinsic pressure of a [[tumor]] mass against the thin-walled [[superior vena cava]] ([[SVC]]) which leads to the development of [[SVC]] syndrome. [[SVC]] syndrome is associated with a number of conditions that include malignant tumors, tuberculosis, histoplasmosis,and syphilis | [[Superior vena cava]] ([[SVC]]) syndrome arises from the obstruction of venous blood drainage of the superior vena cava, which is normally is involved in the major blood flow return from [[head]], [[neck]], upper extremities, and upper thorax to the [[heart]]. Superior vena cava syndrome is a complication from a partial or complete obstruction due to malignant causes (60%) or benign causes (20%). This syndrome may be caused by the invasion of the venous wall associated with intravascular thrombosis, enlarged nodes, enlarged [[ascending aorta]], or more simply, by extrinsic pressure of a [[tumor]] mass against the thin-walled [[superior vena cava]] ([[SVC]]) which leads to the development of [[SVC]] syndrome. [[SVC]] syndrome is associated with a number of conditions that include malignant tumors, tuberculosis, histoplasmosis,and syphilis | ||
== | |||
==Pathogenesis== | |||
The [[superior vena cava]] ([[SVC]]) is the major blood vessel for drainage of venous blood from the [[head]], [[neck]], upper extremities, and upper thorax to the [[heart]]. Knowledge of the anatomy of the [[SVC]] and its relationship to the surrounding [[lymph node]]s is essential to understanding the development of the [[SVC]] syndrome. The [[SVC]] is formed by the junction of the left and right [[brachiocephalic vein]]s in the mid third of the [[mediastinum]]. The [[SVC]] extends caudally for 6 to 8 cm, coursing anterior to the right mainstem [[bronchus]] and terminating in the superior right [[atrium]], and extends anteriorly to the right mainstem bronchus. The [[SVC]] is joined posteriorly by the [[azygos vein]] as it loops over the right mainstem bronchus and lies posterior to and to the right of the [[ascending aorta]]. The mediastinal parietal [[pleura]] is lateral to the [[SVC]], creating a confined space, and the [[SVC]] is adjacent to the right paratracheal, azygous, right hilar, and subcarinal lymph node groups. Obstruction of the [[superior vena cava]] ([[SVC]]) may be caused by neoplastic invasion of the venous wall associated with intravascular thrombosis or, more simply, by extrinsic pressure of a tumor mass against the relatively fixed thin-walled superior vena cava (SVC). The vessel itself is thin-walled, and the blood flowing therein is under low pressure. Thus, when the nodes or [[ascending aorta]] enlarge, the SVC is compressed, blood flow slows, and complete occlusion may occur. | The [[superior vena cava]] ([[SVC]]) is the major blood vessel for drainage of venous blood from the [[head]], [[neck]], upper extremities, and upper thorax to the [[heart]]. Knowledge of the anatomy of the [[SVC]] and its relationship to the surrounding [[lymph node]]s is essential to understanding the development of the [[SVC]] syndrome. The [[SVC]] is formed by the junction of the left and right [[brachiocephalic vein]]s in the mid third of the [[mediastinum]]. The [[SVC]] extends caudally for 6 to 8 cm, coursing anterior to the right mainstem [[bronchus]] and terminating in the superior right [[atrium]], and extends anteriorly to the right mainstem bronchus. The [[SVC]] is joined posteriorly by the [[azygos vein]] as it loops over the right mainstem bronchus and lies posterior to and to the right of the [[ascending aorta]]. The mediastinal parietal [[pleura]] is lateral to the [[SVC]], creating a confined space, and the [[SVC]] is adjacent to the right paratracheal, azygous, right hilar, and subcarinal lymph node groups. Obstruction of the [[superior vena cava]] ([[SVC]]) may be caused by neoplastic invasion of the venous wall associated with intravascular thrombosis or, more simply, by extrinsic pressure of a tumor mass against the relatively fixed thin-walled superior vena cava (SVC). The vessel itself is thin-walled, and the blood flowing therein is under low pressure. Thus, when the nodes or [[ascending aorta]] enlarge, the SVC is compressed, blood flow slows, and complete occlusion may occur. | ||
The severity of the syndrome depends on the rapidity of onset of the obstruction and its location. The more rapid the onset, the more severe the symptoms because the collateral veins do not have time to distend to accommodate an increased blood flow. If the obstruction is above the entry of the [[azygos vein]], the syndrome is less pronounced because the azygous venous system can readily distend to accommodate the shunted blood with less venous pressure developing in the head, arms, and upper thorax. If the obstruction is below the entry of the [[azygos vein]], more florid symptoms and signs are seen because the blood must be returned to the [[heart]] via the upper abdominal veins and the [[inferior vena cava]], which requires higher venous pressure. The general recruitment of venous collateral over time may lead to remission of the syndrome, although the [[SVC]] remains obstructed. | The severity of the syndrome depends on the rapidity of onset of the obstruction and its location. The more rapid the onset, the more severe the symptoms because the collateral veins do not have time to distend to accommodate an increased blood flow. If the obstruction is above the entry of the [[azygos vein]], the syndrome is less pronounced because the azygous venous system can readily distend to accommodate the shunted blood with less venous pressure developing in the head, arms, and upper thorax. If the obstruction is below the entry of the [[azygos vein]], more florid symptoms and signs are seen because the blood must be returned to the [[heart]] via the upper abdominal veins and the [[inferior vena cava]], which requires higher venous pressure. The general recruitment of venous collateral over time may lead to remission of the syndrome, although the [[SVC]] remains obstructed. | ||
==Genetics== | |||
==Associated Conditions== | |||
==Gross Pathology== | |||
==Microscopic Pathology== | |||
==References== | |||
==References== | ==References== | ||
| Line 16: | Line 34: | ||
[[Category:Grammar]] | [[Category:Grammar]] | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Hematology]] | [[Category:Hematology]] | ||
[[Category:Cardiology]] | [[Category:Cardiology]] | ||
Revision as of 18:46, 11 January 2016
|
Superior Vena Cava Syndrome Microchapters |
|
Differentiating Superior Vena Cava Syndrome from Other Diseases |
|---|
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
Superior vena cava syndrome pathophysiology On the Web |
|
American Roentgen Ray Society Images of Superior vena cava syndrome pathophysiology |
|
Directions to Hospitals Treating Superior vena cava syndrome |
|
Risk calculators and risk factors for Superior vena cava syndrome pathophysiology |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Superior vena cava (SVC) syndrome arises from the obstruction of venous blood drainage of the superior vena cava, which is normally is involved in the major blood flow return from head, neck, upper extremities, and upper thorax to the heart. Superior vena cava syndrome is a complication from a partial or complete obstruction due to malignant causes (60%) or benign causes (20%). This syndrome may be caused by the invasion of the venous wall associated with intravascular thrombosis, enlarged nodes, enlarged ascending aorta, or more simply, by extrinsic pressure of a tumor mass against the thin-walled superior vena cava (SVC) which leads to the development of SVC syndrome. SVC syndrome is associated with a number of conditions that include malignant tumors, tuberculosis, histoplasmosis,and syphilis
Pathogenesis
The superior vena cava (SVC) is the major blood vessel for drainage of venous blood from the head, neck, upper extremities, and upper thorax to the heart. Knowledge of the anatomy of the SVC and its relationship to the surrounding lymph nodes is essential to understanding the development of the SVC syndrome. The SVC is formed by the junction of the left and right brachiocephalic veins in the mid third of the mediastinum. The SVC extends caudally for 6 to 8 cm, coursing anterior to the right mainstem bronchus and terminating in the superior right atrium, and extends anteriorly to the right mainstem bronchus. The SVC is joined posteriorly by the azygos vein as it loops over the right mainstem bronchus and lies posterior to and to the right of the ascending aorta. The mediastinal parietal pleura is lateral to the SVC, creating a confined space, and the SVC is adjacent to the right paratracheal, azygous, right hilar, and subcarinal lymph node groups. Obstruction of the superior vena cava (SVC) may be caused by neoplastic invasion of the venous wall associated with intravascular thrombosis or, more simply, by extrinsic pressure of a tumor mass against the relatively fixed thin-walled superior vena cava (SVC). The vessel itself is thin-walled, and the blood flowing therein is under low pressure. Thus, when the nodes or ascending aorta enlarge, the SVC is compressed, blood flow slows, and complete occlusion may occur.
The severity of the syndrome depends on the rapidity of onset of the obstruction and its location. The more rapid the onset, the more severe the symptoms because the collateral veins do not have time to distend to accommodate an increased blood flow. If the obstruction is above the entry of the azygos vein, the syndrome is less pronounced because the azygous venous system can readily distend to accommodate the shunted blood with less venous pressure developing in the head, arms, and upper thorax. If the obstruction is below the entry of the azygos vein, more florid symptoms and signs are seen because the blood must be returned to the heart via the upper abdominal veins and the inferior vena cava, which requires higher venous pressure. The general recruitment of venous collateral over time may lead to remission of the syndrome, although the SVC remains obstructed.