Literature DB >> 12422002

Churg-Strauss syndrome: clinical and serological features of 19 patients from a single Italian centre.

A Della Rossa1, C Baldini, A Tavoni, A Tognetti, D Neglia, G Sambuceti, R Puccini, C Colangelo, S Bombardieri.   

Abstract

OBJECTIVE: Churg-Strauss syndrome is a rare multisystem vasculitis of unknown aetiology. Due to the rarity of the disease, few single-centre case series have been described. The aim of this study was to evaluate a small series from a single Italian centre in order to describe the clinical features of the disease, the treatment and long-term follow-up.
METHODS: Nineteen Churg-Strauss syndrome patients were selected from the medical records of all vasculitis patients attending the Immunology Unit at the Department of Internal Medicine of the University of Pisa in the decade between 1989 and 2000. Data were obtained retrospectively.
RESULTS: All the patients had asthma and hypereosinophilia. As in other case series, the lungs, skin and peripheral nervous system were the most commonly involved organs. The majority of our patient received i.v. pulses of methylprednisolone followed by i.v. pulses of cyclophosphamide. The outcome and long-term follow-up were good. There were no fatalities observed in this series during the follow-up period.
CONCLUSIONS: Churg-Strauss syndrome is a systemic vasculitis occurring in patients with a history of asthma and allergic rhinitis. The positive results of the treatment protocol used in this preliminary study deserve to be tested in controlled multicentre studies.

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Year:  2002        PMID: 12422002     DOI: 10.1093/rheumatology/41.11.1286

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  17 in total

1.  Combination therapy to treat churg-strauss syndrome: corticosteroids with short- or long-term cyclophosphamide pulses.

Authors:  Luis R Espinoza
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2.  Clinical and Serological Features of Eosinophilic and Vasculitic Phases of Eosinophilic Granulomatosis with Poliangiitis: a Case Series of 15 Patients.

Authors:  İnsu Yılmaz; Nuri Tutar; Zuhal Özer Şimşek; Fatma Sema Oymak; İnci Gülmez
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3.  Eosinophilic Lung Disease: Accompanied with 12 Cases.

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4.  urinary biomarkers in relapsing antineutrophil cytoplasmic antibody-associated vasculitis.

Authors:  Jason G Lieberthal; David Cuthbertson; Simon Carette; Gary S Hoffman; Nader A Khalidi; Curry L Koening; Carol A Langford; Kathleen Maksimowicz-McKinnon; Philip Seo; Ulrich Specks; Steven R Ytterberg; Peter A Merkel; Paul A Monach
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5.  Neurologic manifestations of systemic immunopathological diseases.

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6.  Peripheral neuropathy in Wegener's granulomatosis, Churg-Strauss syndrome and microscopic polyangiitis.

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Review 7.  Cutaneous manifestations of Churg-Strauss syndrome: report of two cases and review of the literature.

Authors:  Laura Bosco; Anna Peroni; Donatella Schena; Chiara Colato; Giampiero Girolomoni
Journal:  Clin Rheumatol       Date:  2010-10-15       Impact factor: 2.980

8.  Alveolar haemorrhage in eosinophilic granulomatosis and polyangiitis (Churg-Strauss).

Authors:  L Yalakki Jagadeesh; S R Sangle; H Verma; D D'Cruz
Journal:  Clin Rheumatol       Date:  2014-01-25       Impact factor: 2.980

9.  Peripheral neuropathy as initial manifestation of primary systemic vasculitides.

Authors:  Joachim Wolf; Verena Schmitt; Frederic Palm; Armin J Grau; Raoul Bergner
Journal:  J Neurol       Date:  2012-12-02       Impact factor: 4.849

Review 10.  Eosinophilic granulomatosis with polyangiitis complicated by cholecystitis: a case report and review of the literature.

Authors:  Lu Ye; Xiaoyong Lu; Jing Xue
Journal:  Clin Rheumatol       Date:  2014-02-11       Impact factor: 2.980

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