Literature DB >> 22089070

[Granulomatosis with polyangiitis (Wegener). Description of 15 cases].

Melania Martínez-Morillo1, Dolors Grados, Dolores Naranjo-Hans, Lourdes Mateo, Susana Holgado, Alejandro Olivé.   

Abstract

BACKGROUND: Granulomatosis with polyangiitis (GP) is a necrotizing vasculitis of unknown etiology that involves small and medium caliber vessels. It is associated with anti neutrophil cytoplasm antibodies (ANCA). It most often affects the respiratory tract and the kidneys and its most important pathologic feature is the presence of necrotizing granulomas.
OBJECTIVES: To detail the features of 15 patients with GP diagnosed in a university referral center. PATIENTS AND METHODS: Retrospective study: between 1984 and 2009, 15 patients with GP were diagnosed in our center. Epidemiological, clinical, laboratory test as well as pathologic studies and treatment were retrospectively analyzed. Biopsy diagnosis of GP was considered as an inclusion criterion.
RESULTS: Fifteen patients were diagnosed: 12 men and 3 women. Mean age at diagnosis: 52.2 years (14-78). 12 patients had a history of smoking. A biopsy was diagnostic in all patients. ANCA were positive in 11 cases, 6 had a cytoplasmic c-ANCA pattern. All patients had pulmonary involvement and seven (40%) had renal involvement. All patients received intravenous glucocorticoids and cyclophosphamide as induction therapy. During the disease progression 5 patients died.
CONCLUSIONS: The clinical features of this series do not differ from those described by other authors. However, a history of smoking is more common than expected. Frequently used drugs were glucocorticoids and cyclophosphamide (oral and pulse therapy). The course was usually unfavorable, with outbreaks or complications due to immunosuppression, except for those with limited forms. Immunosuppressive therapy should be maintained indefinitely in most cases.
Copyright © 2010 Elsevier España, S.L. All rights reserved.

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Year:  2011        PMID: 22089070     DOI: 10.1016/j.reuma.2011.04.009

Source DB:  PubMed          Journal:  Reumatol Clin        ISSN: 1699-258X


  4 in total

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Journal:  Rheumatol Int       Date:  2014-05-18       Impact factor: 2.631

2.  Temporal and Cartographic Analyses of the Distribution within Spain of Mortality Due to Granulomatosis with Polyangiitis (1984⁻2016).

Authors:  Germán Sánchez-Díaz; Francisco Escobar; Ana Villaverde-Hueso; Manuel Posada de la Paz; Verónica Alonso-Ferreira
Journal:  Int J Environ Res Public Health       Date:  2019-04-17       Impact factor: 3.390

3.  Granulomatosis with polyangiitis: clinical course and outcome of 60 patients from a single center in South India.

Authors:  Vineeta Shobha; Saba Fathima; Ravi Prakash
Journal:  Clin Exp Med       Date:  2018-02-28       Impact factor: 3.984

4.  Multiple Bullous and Ulcers as Cutaneous Manifestations of Wegener's Granulomatosis: A Rare Case Report.

Authors:  Miranti Pangastuti; Trustia Rizqandaru; Oki Suwarsa; Hartati Purbo Dharmadji; Endang Sutedja
Journal:  Clin Cosmet Investig Dermatol       Date:  2022-10-07
  4 in total

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