Pregnancy complicating Wegener's granulomatosis

Author:

Soh May Ching1,Hart Hamish H2,Bass Eileen3,Wilkinson Lucille3

Affiliation:

1. North Shore Hospital, Waitemata District Health Board, Auckland, New Zealand

2. North Shore Hospital, North Shore City, Auckland, New Zealand

3. National Women's Health, Auckland City Hospital, Auckland District Health Board, Auckland, New Zealand

Abstract

Pregnancy associated with Wegener's granulomatosis is rare. Therapeutic options are limited. There is a paucity of published literature to guide clinical decision-making in these complex patients. Two cases are presented. Firstly, a 33-year-old woman with generalized Wegener's in remission and off all medications presented with a flare in the third trimester with haemoptysis, raised C-reactive protein and c-anti-neutrophilic cytoplasmic antibody (c-ANCA) levels. Her care was complicated by florid steroid-induced psychosis. With deteriorating disease control, she was treated with pulsed-intravenous cyclophosphamide with a good response. She delivered a healthy baby at 38 weeks. She had a severe postpartum flare. Secondly, a 37-year-old woman with limited Wegener's in remission for the last two years and off all treatment became pregnant after pre-conception counselling. A normal baby was delivered at term. An exhaustive review of all published literature on Wegener's activity in pregnancy is presented along with therapeutic options and recommendations.

Publisher

SAGE Publications

Subject

Obstetrics and Gynecology

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