Heliyon (Oct 2022)

Case report of rare congenital cardiovascular anomalies associated with truncus arteriosus type 2

  • Leona S. Alizadeh,
  • Vitali Koch,
  • Leon D. Grünewald,
  • Ibrahim Yel,
  • Daniel Mathies,
  • Dominic Rauschning,
  • Thomas J. Vogl,
  • Christian Booz

Journal volume & issue
Vol. 8, no. 10
p. e11033

Abstract

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Truncus arteriosus (TA) is a very rare congenital anomaly with complex cardiovascular anatomy and high lethality also due to severe associated anatomical variants and pathologies. As TA has a massive impact on the survival of a newborn and usually has to be surgically treated. Thus, it is of high importance to understand this congenital cardiovascular disease and associated complications, to improve life expectancy and outcome of these patients. We recently came across a newborn female patient with a rare complex case of persistent TA type 2 associated with further complex cardiovascular anomalies, who received a contrast enhanced CT scan on the 3 rd day post-partum, showing complex cardiovascular abnormalities that were ultimately incompatible with life.

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