ChloroquineV1, Main, Exploration, bibRecord, 001C57

Spontaneous pneumomediastinum and dermatomyositis may be a not so rare association: report of a case and review of the literature

Identifieur interne : 001C57 ( Main/Exploration ); précédent : 001C56; suivant : 001C58

Spontaneous pneumomediastinum and dermatomyositis may be a not so rare association: report of a case and review of the literature

Auteurs : Fabricio De Souza Neves [Brésil] ; Samuel Katsuyuki Shinjo [Brésil] ; Jozélio Freire Carvalho [Brésil] ; Maurício Levy-Neto [Brésil] ; Cláudia Tereza Lobato Borges [Brésil]

Source :

Clinical Rheumatology [ 0770-3198 ] ; 2007-01-01.

RBID : ISTEX:9CCE2A127CF232806EF9340BB5FFBB32258D312A

English descriptors

KwdEn :
- Dermatomyositis, Lung, Mediastinal emphysema, Myositis, Vasculitis.

Abstract

Abstract: One patient with dermatomyositis (DM) who developed spontaneous pneumomediastinum (SPnM) is described. A review of 15 previously reported cases shows that this is a complication of DM but not of polymyositis. It occurs in young patients with recent onset of disease characterized by cutaneous vasculopathy, and patients treated with immunosuppressive drugs have, in general, better outcomes. We suggest that the onset of SPnM in DM patients must alert to possible vasculitic activity and that immunosuppressive agents with progressive tapering of corticosteroids are part of the most reasonable approach in these cases.

Url:

https://api.istex.fr/ark:/67375/VQC-V81K8844-Z/fulltext.pdf

DOI: 10.1007/s10067-005-0109-x

Affiliations:

Links toward previous steps (curation, corpus...)

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to stream Main, to step Curation: 001C57

Le document en format XML

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<idno type="ISSN">0770-3198</idno>
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<front><div type="abstract" xml:lang="en">Abstract: One patient with dermatomyositis (DM) who developed spontaneous pneumomediastinum (SPnM) is described. A review of 15 previously reported cases shows that this is a complication of DM but not of polymyositis. It occurs in young patients with recent onset of disease characterized by cutaneous vasculopathy, and patients treated with immunosuppressive drugs have, in general, better outcomes. We suggest that the onset of SPnM in DM patients must alert to possible vasculitic activity and that immunosuppressive agents with progressive tapering of corticosteroids are part of the most reasonable approach in these cases.</div>
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Spontaneous pneumomediastinum and dermatomyositis may be a not so rare association: report of a case and review of the literature

Spontaneous pneumomediastinum and dermatomyositis may be a not so rare association: report of a case and review of the literature

Source :

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri