Abetalipoproteinemia complicating the puerperium

Obstet Gynecol. 2008 Feb;111(2 Pt 2):575-7. doi: 10.1097/01.AOG.0000295869.92443.ce.

Abstract

Background: Abetalipoproteinemia is a rare, autosomal recessive disease, in which the absence of beta-lipoprotein results in the malabsorption of fat-soluble vitamins. There are few reported complications from abetalipoproteinemia during pregnancy. We present a case of untreated abetalipoproteinemia complicating the puerperium.

Case: A 23-year-old, gravida 3, para 0020 woman presented to an outside facility in labor, and her delivery was complicated by postpartum hemorrhage and a large vulvar hematoma. She was coagulopathic and transferred for suspected disseminated intravascular coagulation. Her preexisting medical history was not appreciated by the transferring facility.

Conclusion: Abetalipoproteinemia in pregnancy is rare. Untreated disease conveys multi-system organ dysfunction and has ramifications in labor and delivery. Clinicians must elicit a comprehensive medical history to properly manage complications in the puerperium.

Publication types

  • Case Reports

MeSH terms

  • Abetalipoproteinemia / complications
  • Abetalipoproteinemia / diagnosis*
  • Abetalipoproteinemia / therapy*
  • Adult
  • Disseminated Intravascular Coagulation / diagnosis
  • Disseminated Intravascular Coagulation / etiology
  • Disseminated Intravascular Coagulation / therapy
  • Female
  • Humans
  • Puerperal Disorders / diagnosis*
  • Puerperal Disorders / etiology
  • Puerperal Disorders / therapy*