TY - JOUR
T1 - Persistent left superior vena cava with absent right superior vena cava: Morphological CT features and clinical implications
AU - Heye, Tobias
AU - Wengenroth, Martina
AU - Schipp, Anne
AU - Johannes Dengler, Thomas
AU - Grenacher, Lars
AU - Werner Kauffmann, Günter
PY - 2007/4/4
Y1 - 2007/4/4
N2 - Here we report a rare case of the persisting left superior vena cava with simultaneous absence of the right superior vena cava. This central venous variation has been identified during a routine chest CT scan as follow-up after colonic cancer in an asymptomatic patient with no previous history of heart diseases. Morphological features of this variation are illustrated on axial CT images and 3D image reconstructions. This anomaly occurs in 0.1% of the general population. In presence with the right superior vena cava it is the most common anatomical variation in the central venous system with a reported occurrence of 0.2-8%. Such condition can be associated with additional congenital cardiovascular malformations and heart diseases or rhythm abnormalities. Diagnosis can be difficult and is often achieved incidentally since hemodynamics in these patients can be normal and clinical symptoms are mostly absent. Important clinical implications include difficulties in central venous access or cardiac pacemaker placement as well as management consequences in cardiothoracic surgery. In conclusion clinicians should be aware of this anomaly and their clinical relevance to avoid possible complications.
AB - Here we report a rare case of the persisting left superior vena cava with simultaneous absence of the right superior vena cava. This central venous variation has been identified during a routine chest CT scan as follow-up after colonic cancer in an asymptomatic patient with no previous history of heart diseases. Morphological features of this variation are illustrated on axial CT images and 3D image reconstructions. This anomaly occurs in 0.1% of the general population. In presence with the right superior vena cava it is the most common anatomical variation in the central venous system with a reported occurrence of 0.2-8%. Such condition can be associated with additional congenital cardiovascular malformations and heart diseases or rhythm abnormalities. Diagnosis can be difficult and is often achieved incidentally since hemodynamics in these patients can be normal and clinical symptoms are mostly absent. Important clinical implications include difficulties in central venous access or cardiac pacemaker placement as well as management consequences in cardiothoracic surgery. In conclusion clinicians should be aware of this anomaly and their clinical relevance to avoid possible complications.
UR - http://www.scopus.com/inward/record.url?scp=33847119001&partnerID=8YFLogxK
U2 - 10.1016/j.ijcard.2006.08.067
DO - 10.1016/j.ijcard.2006.08.067
M3 - Journal articles
C2 - 17101181
AN - SCOPUS:33847119001
SN - 0167-5273
VL - 116
SP - e103-e105
JO - International Journal of Cardiology
JF - International Journal of Cardiology
IS - 3
ER -