Familial peripartum cardiomyopathy after molar pregnancy

Obstet Gynecol. 1993 May;81(5 ( Pt 2)):886-8.

Abstract

Background: The potential complications of molar pregnancy are numerous and well defined, but associated peripartum cardiomyopathy has not been reported.

Case: A 16-year-old primigravida with a family history of peripartum cardiomyopathy requiring cardiac transplantation underwent suction curettage of a complete mole at 12 weeks' gestation. Three months after evacuation, she developed congestive heart failure. Radionuclide ventriculography demonstrated an ejection fraction of 30%, echocardiography revealed enlargement and ventricular hypokinesis, and a myocardial biopsy specimen contained hypertrophy and fibrosis without necrosis or active inflammation. The patient improved with medical therapy.

Conclusion: Peripartum cardiomyopathy is a potential complication of molar pregnancy. In spite of the poor prognosis sometimes reported for this disease, good functional outcome may follow.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Cardiomyopathy, Dilated / diagnosis
  • Cardiomyopathy, Dilated / etiology*
  • Cardiomyopathy, Dilated / therapy
  • Family
  • Female
  • Humans
  • Hydatidiform Mole / complications*
  • Pregnancy
  • Puerperal Disorders / diagnosis
  • Puerperal Disorders / etiology*
  • Puerperal Disorders / therapy
  • Uterine Neoplasms / complications*