Small vessel vasculitis and relapsing panniculitis in tumour necrosis factor receptor associated periodic syndrome (TRAPS)

P. Lamprecht*, F. Moosig, S. Adam-Klages, U. Mrowietz, E. Csernok, M. Kirrstetter, K. Ahmadi-Simab, J. O. Schroder, W. L. Gross

*Corresponding author for this work
64 Citations (Scopus)

Abstract

Case reports: A 66 year old female patient had relapsing fever and non-suppurative panniculitis suggestive of enigmatic "Weber-Christian disease" (WCD). Antineutrophil cytoplasmic antibodies with specificity for human leucocyte elastase (HLE-ANCA) were detected. A biopsy showed small vessel vasculitis and panniculitis. A 53 year old man had recurrent episodes of abdominal pain, erythematous rash, and myalgia. Fever attacks had stopped a few years ago. A biopsy showed panniculitis and fasciitis. In both patients mutations (R92Q, T50M) of the tumour necrosis factor receptor super family (TNFRSF) 1A gene were disclosed. Mutations of the TNFRSF 1A gene are the cause of tumour necrosis factor receptor associated, periodic syndrome (TRARS). Both patients responded favourably to treatment with the human soluble p75 TNFα receptor fusion protein etanercept (2×25 mg subcutaneously/week). Discussion: Small vessel vasculitis and panniculitis have not been reported in TRAPS so far. The cases underline the importances of TNFα regulation in inflammatory processes including vasculitis. Genetically determined causes of fever may account for some cases or WCD.

Original languageEnglish
JournalAnnals of the Rheumatic Diseases
Volume63
Issue number11
Pages (from-to)1518-1520
Number of pages3
ISSN0003-4967
DOIs
Publication statusPublished - 11.2004

Research Areas and Centers

  • Academic Focus: Center for Infection and Inflammation Research (ZIEL)

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