Inferior Vena Cava Agenesis: An Underrated Cause of Deep Venous Thrombosis.
agenesis
collateral veins
deep vein thrombosis (dvt)
inferior vena cava
ivc embryology
Journal
Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737
Informations de publication
Date de publication:
Jan 2023
Jan 2023
Historique:
accepted:
10
01
2023
entrez:
16
2
2023
pubmed:
17
2
2023
medline:
17
2
2023
Statut:
epublish
Résumé
The absence of the inferior vena cava (IVC) is a rare abnormality reported in less than 1% of the population. The condition is usually the result of defects during embryogenesis. The collateral veins are enlarged with agenesis IVC, enabling blood transport to the superior vena cava. Although the alternate pathways enable venous drainage of the lower extremities, IVC agenesis (IVCA) may predispose to venous hypertension and complications, including thromboembolism. This report includes a case of a 35-year-old obese male who presented with deep vein thrombosis (DVT) in his left lower extremity (LLE) with no predisposing factors, which led to an incidental discovery of the inferior vena cava agenesis. Imaging showed thrombosis of the deep veins of the LLE, absence of the IVC, enlarged paralumbar veins, filling of the superior vena cava, and left renal atrophy. The patient responded to therapeutic heparin infusion, and catheter placement and thrombectomy were performed. The patient was discharged on the third day with medications and vascular follow-up. It is essential to recognize the complications of IVCA and its correlation with other findings, such as atrophy of the kidney. The agenesis of IVC is a highly under-recognized cause of DVT of the lower extremities in the young population without other risk factors. Hence, a complete diagnostic evaluation is necessary for this age group, including imaging for vascular anomalies, besides the thrombophilic screening.
Identifiants
pubmed: 36793843
doi: 10.7759/cureus.33667
pmc: PMC9924708
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e33667Informations de copyright
Copyright © 2023, Kannappan et al.
Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
Références
Br J Haematol. 2002 Sep;118(4):1199-200
pubmed: 12199817
J Radiol Case Rep. 2014 Apr 01;8(4):38-47
pubmed: 24967034
QJM. 2018 Feb 1;111(2):117-118
pubmed: 29186563
Am Surg. 2005 Jun;71(6):502-4
pubmed: 16044930
AJR Am J Roentgenol. 2003 Mar;180(3):729-32
pubmed: 12591684
Br J Radiol. 1974 Apr;47(556):206-13
pubmed: 4824552
Vasc Med. 2010 Dec;15(6):451-9
pubmed: 21183652
Insights Imaging. 2014 Oct;5(5):619-28
pubmed: 25171956
Case Rep Vasc Med. 2015;2015:651436
pubmed: 26788400
J Vasc Surg. 2006 Aug;44(2):416
pubmed: 16890880
Lancet. 2001 Feb 10;357(9254):441
pubmed: 11273066
J Med Case Rep. 2008 Feb 12;2:46
pubmed: 18269760
Yonsei Med J. 2004 Oct 31;45(5):947-51
pubmed: 15515211
Cardiovasc Diagn Ther. 2016 Dec;6(6):482-492
pubmed: 28123970
J Pediatr. 1961 Sep;59:370-83
pubmed: 13683264