Your browser doesn't support javascript.
loading
Infrarenal inferior vena cava agenesis and recurrent deep vein thrombosis: a case report and literature review.
Prado, Victor E; Rey-Mendoza, Juan Pablo; Wakefield, Connor J; Aqeel, Sheeba Ba; Kumssa, Admasu.
Afiliação
  • Prado VE; Division of Internal Medicine, Department of Medicine, University of Cincinnati, Cincinnati, OH, USA.
  • Rey-Mendoza JP; Division of Pulmonary and Critical Care, Department of Medicine, University of Wisconsin, Madison, WI, USA.
  • Wakefield CJ; Department of Medicine, Rush Medical College, Chicago, IL, USA.
  • Aqeel SB; Division of Internal Medicine, Department of Medicine, John H. Stroger, Jr. Hospital of Cook County, Chicago, IL, USA.
  • Kumssa A; Division of Internal Medicine, Department of Medicine, John H. Stroger, Jr. Hospital of Cook County, Chicago, IL, USA.
Oxf Med Case Reports ; 2021(1): omaa104, 2021 Jan.
Article em En | MEDLINE | ID: mdl-33469470
Inferior vena cava agenesis is a rare congenital vascular defect often diagnosed as an incidental finding in asymptomatic patients. When symptoms arise, it can present with chronic venous stasis or unprovoked deep vein thrombosis (DVT). A 42-year-old man with history of unprovoked right lower extremity (RLE) DVTs was admitted for swelling, pain and erythema to the RLE, concerning for new DVT. Venous Doppler ultrasound showed a chronic DVT of the right proximal femoral vein in addition to an acute DVT of the distal femoral vein. Extensive thrombophilia workup was negative and additional imaging with abdominal computed tomography scan revealed the absence of the infrarenal inferior vena cava. Patient was treated with oral anticoagulation and compression stockings and discharged with clinical improvement. At 3-month follow-up, patient was completely asymptomatic. Recurrent unprovoked DVTs in young patients require exhaustive work up including imaging studies to rule out vascular anomalies.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article