A case of unusual visceral heterotaxy syndrome with isolated levocardia

Dae Sun Jo1, Sung Su Jung, Chan Uhng Joo

  • 1Department of Pediatrics, Chonbuk National University Medical School, Jeonju, Korea.

Korean Circulation Journal
|November 21, 2013
PubMed

Insights

Situs inversus with isolated levocardia is rare, often linked to heart defects. This case details a 19-year-old male with situs inversus and a normal heart, presenting unique abdominal and splenic findings.

Area of Science:

  • Medical Imaging
  • Human Anatomy
  • Rare Diseases

Background:

  • Situs inversus with isolated levocardia is a rare congenital condition.
  • It is typically associated with significant cardiac anomalies.
  • This presentation describes an unusual asymptomatic case.

Purpose of the Study:

  • To report a rare case of situs inversus with isolated levocardia.
  • To highlight the absence of congenital heart defects in this specific case.
  • To document associated abdominal and splenic abnormalities.

Main Methods:

  • Spiral computed tomography (CT) of the thorax and abdomen.
  • Echocardiographic studies.
  • Clinical case review.

Main Results:

  • Confirmed situs inversus of abdominal organs and normal heart position (levocardia).
  • Observed mirrored left lungs, midline liver, and left-sided inferior vena cava.
  • Identified multiple splenic masses and splenic artery aneurysmal dilatation.

Conclusions:

  • Situs inversus with isolated levocardia can occur without severe congenital heart defects.
  • This case demonstrates unusual splenic and vascular anomalies.
  • Further investigation into the spectrum of this rare condition is warranted.

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