Literature DB >> 7653948

Gastrointestinal tract involvement in polyarteritis nodosa and Churg-Strauss syndrome.

L Guillevin1, F Lhote, V Gallais, B Jarrousse, I Royer, M Gayraud, J Benichou.   

Abstract

OBJECTIVE: To study the nature and incidence of gastrointestinal (GI) manifestations in polyarteritis nodosa (PAN) and Churg-Strauss syndrome (CSS) and define their therapeutic and prognostic implications.
METHODS: Fifty-three patients (29 males, 24 females) affected with PAN or CSS and followed in our institution were included in a retrospective study. Patients were divided into 2 groups: patients without GI manifestations (group A) and patients with GI manifestations (group B). Among patients with GI manifestations we have studied a subgroup with a possibly poorer prognosis in whom the following symptoms were present: GI tract hemorrhage, intestinal perforation, digestive tract surgery due to PAN manifestations, intractable abdominal pain and weight loss greater than 20% of normal weight due to GI tract ischemia.
RESULTS: The clinical manifestations were those that are classically encountered in PAN and CSS. Every patient fulfilled the American College of Rheumatology (ACR) criteria for PAN and CSS. Thirty-five patients without GI manifestations were included in group A and 18 patients (34%) with GI manifestations in group B. The mean age of the group at the time of diagnosis was 56.9 +/- 19.1 years (range: 21-71 years) in group A and 47.5 +/- 16.8 years (range: 12-82) in group B. GI manifestations were considered as one of the symptoms revealing PAN in 7 (13.2%) cases. Six of the 18 patients with GI manifestations had definite organ involvement related to vasculitis. Abdominal pain without characteristic organ involvement or surgical emergency was present in 12/18 patients. HBV infection was more frequently observed in group B than in group A. Survival curves showed that at 10 years, 80% of the patients in group A were alive versus 67% in group B (P not significant). For the 9 patients with severe GI manifestations, the survival curves showed that, at 10 years, 44% of them were alive versus 80% in the other group A (p < 0.001).
CONCLUSIONS: GI manifestations are frequent in PAN and CSS and were present in 34% of our patients. Prognosis of PAN with GI manifestations is not statistically different than in PAN without GI involvement, except for patients with severe digestive complications.

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Year:  1995        PMID: 7653948

Source DB:  PubMed          Journal:  Ann Med Interne (Paris)        ISSN: 0003-410X


  5 in total

Review 1.  Polyarteritis nodosa and microscopic polyangiitis: etiologic and diagnostic considerations.

Authors:  Laura B Hughes; S Louis Bridges
Journal:  Curr Rheumatol Rep       Date:  2002-02       Impact factor: 4.592

2.  A case of polyarteritis nodosa with lesions of the superior mesenteric artery illustrating the diagnostic usefulness of three-dimensional computed tomographic angiography.

Authors:  Takashi Kato; Kenji Fujii; Eiji Ishii; Ryoichi Wada; Yuji Hidaka
Journal:  Clin Rheumatol       Date:  2005-07-26       Impact factor: 2.980

3.  Acute cholecystitis at initial presentation of polyarteritis nodosa.

Authors:  Sandra Regina Muchinechi Fernandes; Adil Muhib Samara; Eduardo Paiva Magalhães; Zoraida Sachetto; Konradin Metze
Journal:  Clin Rheumatol       Date:  2005-03-24       Impact factor: 2.980

Review 4.  Cutting edge issues in the Churg-Strauss syndrome.

Authors:  Wojciech Szczeklik; Bogdan Jakieła; Dariusz Adamek; Jacek Musiał
Journal:  Clin Rev Allergy Immunol       Date:  2013-02       Impact factor: 8.667

5.  Hepatic involvement in Wegener's granulomatosis: a case report.

Authors:  Constantin Goritsas; Nicolas P Paissios; Rodoula Trigidou; Joanna Delladetsima
Journal:  J Med Case Rep       Date:  2010-01-14
  5 in total

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