Literature DB >> 7774112

Schnitzler's syndrome (urticaria and macroglobulinemia) dramatically improved with corticosteroids.

P Goupille1, P Pizzuti, E Diot, F Jattiot, J L Guilmot, J P Valat.   

Abstract

The authors report the case of a 65-year-old man who had an evolving case of Schnitzler's syndrome with lytic bone lesions which was unresponsive to several drugs, and which dramatically improved with small quantities of corticosteroids. Schnitzler's syndrome, first described in 1974, is defined by chronic non-pruritic urticaria, osteocondensation, and monoclonal IgM dysproteinemia without features of lymphoproliferative disease, and is associated with fever, deterioration of the general health and biological signs of inflammation. Only 22 cases of Schnitzler's syndrome have been reported hitherto and there is no known effective treatment, H1 and H2 blockers, dapsone, colchicine, chloroquine, cyclophosphamide, chlorambucil and azathioprine having proven useless in the few patients treated. Corticosteroids may be effective, however, especially against the urticaria.

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Year:  1995        PMID: 7774112

Source DB:  PubMed          Journal:  Clin Exp Rheumatol        ISSN: 0392-856X            Impact factor:   4.473


  4 in total

1.  Schnitzler's syndrome: 3-year radiological follow-up.

Authors:  A Bertrand; A Feydy; N Belmatoug; B Fantin
Journal:  Skeletal Radiol       Date:  2006-04-07       Impact factor: 2.199

2.  Radiotherapy for a breast cancer patient with Schnitzler syndrome: Report of acute toxicity and early follow-up.

Authors:  Samir Abdallah Hanna; Ana Luisa Garcia Calich; Artur Katz; Isidio Calich; Gustavo Gibin Duarte; José Luiz Barbosa Bevilacqua
Journal:  Rep Pract Oncol Radiother       Date:  2017-09-08

Review 3.  The Schnitzler syndrome.

Authors:  Dan Lipsker
Journal:  Orphanet J Rare Dis       Date:  2010-12-08       Impact factor: 4.123

4.  Schnitzler's syndrome: a case report.

Authors:  Gabriel Tinoco; Rehan Kanji; Deepthi Moola
Journal:  Case Rep Med       Date:  2013-06-09
  4 in total

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