Multivisceral Fibromuscular Dysplasia in Childhood: Case Report and Review of the Literature

Wilhelm Sandmann*, Klaus-Martin Schulte

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)

Abstract

We report here a 9-year-old girl with fibromuscular dysplasia of many muscular arteries including both renal and internal carotid arteries, the celiac artery, superior mesenteric artery, and one external carotid artery. She suffered from severe renovascular hypertension with beginning secondary cardiac decompensation, typical angina abdominalis, and neurological signs, including severe headaches and hemianopsia. Surgery was performed for all major vessels and the outcome is good 2.5 years after the operation. The clinical presentation, differential diagnosis, and treatment options of fibromuscular dysplasia in childhood are discussed and the literature is reviewed.

Original languageEnglish
Pages (from-to)496-502
Number of pages7
JournalAnnals of Vascular Surgery
Volume14
Issue number5
DOIs
Publication statusPublished - Sept 2000
Externally publishedYes

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