Multiple and recurrent systemic thrombotic events associated with congenital anomaly of inferior vena cava

Naohumi Takehara1, Naoyuki Hasebe, Setsu Enomoto

  • 1The first Department of Medicine, Asahikawa Medical College, Asahikawa, Japan. takenao@asahikawa-med.ac.jp

Insights

A rare congenital absence of the infra-renal inferior vena cava was diagnosed in a patient with acute myocardial infarction and deep vein thrombosis. This anatomical variation may predispose individuals to venous thromboembolism.

Area of Science:

  • Vascular Surgery
  • Cardiology
  • Radiology

Background:

  • Inferior vena cava (IVC) anomalies are rare congenital conditions.
  • Thrombosis is a common clinical problem, often associated with risk factors like immobility and genetic predisposition.

Observation:

  • A 67-year-old woman with a history of cerebral infarction and pulmonary embolism presented with chest pain.
  • Diagnosis of acute myocardial infarction and deep vein thrombosis (DVT) was established.
  • Imaging revealed congenital absence of the infra-renal IVC, with venous drainage rerouted through an ascending lumbar vein.

Findings:

  • The patient's presentation of acute myocardial infarction and DVT occurred in the context of a rare congenital IVC anomaly.
  • Congenital absence of the infra-renal IVC is associated with altered venous hemodynamics.
  • The ascending lumbar vein served as an alternative drainage pathway for lower extremity venous return.

Implications:

  • This case highlights the importance of considering rare anatomical variations in the diagnosis of thromboembolic events.
  • Congenital IVC anomalies may represent an underrecognized risk factor for venous thromboembolism.
  • Further research is warranted to elucidate the precise mechanisms linking IVC anomalies to thrombosis.

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