Massive vulvar edema revealing idiopathic systemic capillary leak syndrome

Arch Gynecol Obstet. 2022 Nov;306(5):1795-1797. doi: 10.1007/s00404-022-06740-9. Epub 2022 Aug 16.

Abstract

Idiopathic systemic capillary leak syndrome is a rare disease characterized by recurrent episodes of hypotension, hypoalbuminemia and peripheral edema caused by capillary hyperpermeability with approximately 350 documented cases worldwide. We report herein the case of a 22-year-old primiparous patient with an unusual compartment syndrome represented with spontaneous massive vulvar edema. Treatment consisted of volume replacement and intravenous polyvalent immunoglobulins perfusions. Vulvar edema was treated surgically by incision and drainage with favorable outcome. The pregnancy follow-up did not show any fetal abnormalities. The childbirth at 35 weeks was natural and the newborn was healthy.

Keywords: Critical care; Idiopathic systemic capillary leak syndrome; Intravenous immunoglobulins; Pregnancy; Shock; Vulvar edema.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Capillary Leak Syndrome* / complications
  • Capillary Leak Syndrome* / diagnosis
  • Capillary Leak Syndrome* / therapy
  • Compartment Syndromes* / complications
  • Edema / etiology
  • Humans
  • Hypoalbuminemia* / complications
  • Immunoglobulins, Intravenous
  • Infant, Newborn
  • Young Adult

Substances

  • Immunoglobulins, Intravenous