An (In)Significant Ventricular Septal Defect and/or Double-Chambered Right Ventricle: Are There Any Differences in Diagnosis and Prognosis in Adult Patients

Cardiology. 2016;134(3):375-80. doi: 10.1159/000444743. Epub 2016 Apr 26.

Abstract

A double-chambered right ventricle (DCRV) is an uncommon congenital anomaly: the right ventricle (RV) is divided into two chambers due to the presence of an abnormally located muscular band or anomalous muscle hypertrophy in the subinfundibular part of RV outflow tract, with a variable degree of obstruction. Generally, DCRV is well recognized in childhood and misdiagnosed in adult patients. Transthoracic and/or transesophageal echocardiography are the mx0435;thods of choice for the diagnosis of DCRV. Due to limitations of echocardiography in adult patients, this entity may be missed, particularly if it presents concomitant with other congenital defects, and therefore additional imaging methods such as MRI or cardiac catheterization are required for a definitive diagnosis.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Female
  • Heart Defects, Congenital / diagnosis*
  • Heart Defects, Congenital / physiopathology
  • Heart Defects, Congenital / therapy
  • Heart Septal Defects, Ventricular / diagnosis*
  • Heart Septal Defects, Ventricular / physiopathology
  • Heart Septal Defects, Ventricular / therapy
  • Heart Ventricles / abnormalities*
  • Humans
  • Male
  • Middle Aged
  • Prognosis
  • Young Adult