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Severe hidradenitis suppurativa complicated by renal AA amyloidosis

Utrera-Busquets, M. ; Romero-Maté, A. ; Castaño, Á. ; Alegre, L. ; García-Donoso, C. ; Borbujo, J.

Clinical and experimental dermatology, 2016-04, Vol.41 (3), p.287-289 [Periódico revisado por pares]

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Título:
Severe hidradenitis suppurativa complicated by renal AA amyloidosis
Autor: Utrera-Busquets, M. ; Romero-Maté, A. ; Castaño, Á. ; Alegre, L. ; García-Donoso, C. ; Borbujo, J.
Assuntos: Adult ; Amyloidosis - etiology ; Chronic Disease ; Female ; Hidradenitis Suppurativa - complications ; Humans ; Kidney Diseases - etiology ; Nephrotic Syndrome - etiology
É parte de: Clinical and experimental dermatology, 2016-04, Vol.41 (3), p.287-289
Notas: istex:2FC041190E7C31F3D9955650E17E14021653A11D
ArticleID:CED12731
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ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
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ObjectType-Report-1
ObjectType-Article-3
Descrição: Summary Hidradenitis suppurativa (HS) is a chronic, recurrent inflammatory disease affecting the skin folds. Multiple therapeutic options have been proposed for severe cases, but persistent responses are rarely seen. Important complications of HS are uncommon, and usually seen only in severe and unresponsive disease. Amyloid A (AA) amyloidosis is secondary to inflammatory chronic diseases, and is an uncommon complication of dermatological diseases. Only a few cases related with HS have been reported. We report the case of a 37‐year‐old patient who developed AA amyloidosis secondary to severe HS.
Editor: England: Blackwell Publishing Ltd
Idioma: Inglês

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