Granulomatosis with polyangiitis and pregnancy: Anti-neutrophil cytoplasmic antibody, placental inflammation, chorangiosis and pre-eclampsia

J Obstet Gynaecol Res. 2020 Sep;46(9):1907-1910. doi: 10.1111/jog.14356. Epub 2020 Jul 1.

Abstract

Granulomatosis with polyangiitis (GPA) is a rare necrotizing autoimmune disease involving small vessel vasculitis. Pregnancies with GPA have increased rates of obstetric complications including pre-eclampsia. Differential diagnosis of GPA flares up and pre-eclampsia may be difficult and necessitates careful clinical practice. A 26-year-old pregnant woman with GPA was referred for hypertension. The absence of GPA signs and symptoms, negative anti-neutrophil cytoplasmic antibody titer and the presence of clinical and laboratory findings supported the diagnosis of pre-eclampsia rather than a GPA flare-up. The newborn was delivered via cesarean section at the 30th gestational week due to severe superimposed pre-eclampsia. Pathological examination of the placenta demonstrated the presence of chorangiosis and focal placental infarcts. GPA should be considered as a risk factor in pregnancy and requires careful clinical management to have good gestational outcome. Physicians should be vigilant regarding gestational diabetes and pre-eclampsia as well as GPA flare-up.

Keywords: Wegener's granulomatosis; chorangiosis; granulomatosis with polyangiitis; pre-eclampsia; pregnancy.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antibodies, Antineutrophil Cytoplasmic
  • Cesarean Section
  • Female
  • Granulomatosis with Polyangiitis* / diagnosis
  • Humans
  • Infant, Newborn
  • Inflammation
  • Placenta
  • Pre-Eclampsia* / diagnosis
  • Pregnancy

Substances

  • Antibodies, Antineutrophil Cytoplasmic