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[斯内登-威尔金森病：一例报告]

[Sneddon-Wilkinson disease: a case report].

作者信息

Kerroum Sara, Ammar Najoua, Znati Kaoutar, Ismaili Nadia, Meziane Mariame, Benzekri Laila, Senouci Karima

机构信息

Centre Hospitalier Universitaire Ibn Sina, Service de Dermatologie-Vénérologie, Faculté de Médecine et de Pharmacie, Université Mohamed V, Rabat, Maroc.

Centre Hospitalier Universitaire Ibn Sina, Service d´Anatomo-Pathologie, Faculté de Médecine et de Pharmacie, Université Mohamed V, Rabat, Maroc.

出版信息

Pan Afr Med J. 2022 Nov 1;43:115. doi: 10.11604/pamj.2022.43.115.33116. eCollection 2022.

DOI:10.11604/pamj.2022.43.115.33116
PMID:36721471
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9860085/
Abstract

Sneddon-Wilkinson disease is a benign amicrobial pustulosis belonging to the spectrum of neutrophilic dermatoses. It is characterized by evident stereotypic clinical features, including, in most cases, pustular lesions of the trunk and prominent skin folds. This pustulosis may be associated with other diseases (IgA monoclonal gammopathy, rheumatoid arthritis, neoplasms or other neutrophilic dermatoses) and therefore requires regular follow-up. This disease has a relapsing-remitting course. First line therapy is dapsone. We here report the case of a 49-year-old patient with amicrobial pustulosis (Sneddon-Wilkinson disease).

摘要

斯内登-威尔金森病是一种属于嗜中性皮病谱的良性无菌性脓疱病。其特征为具有明显的刻板临床特征，在大多数情况下包括躯干的脓疱性病变和明显的皮肤褶皱。这种脓疱病可能与其他疾病（IgA单克隆丙种球蛋白病、类风湿性关节炎、肿瘤或其他嗜中性皮病）相关，因此需要定期随访。该病呈复发-缓解病程。一线治疗药物是氨苯砜。我们在此报告一例49岁无菌性脓疱病（斯内登-威尔金森病）患者的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b32/9860085/b0164d58c2da/PAMJ-43-115-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b32/9860085/70ffb77f88b7/PAMJ-43-115-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b32/9860085/728960364b31/PAMJ-43-115-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b32/9860085/c87debb10644/PAMJ-43-115-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b32/9860085/b0164d58c2da/PAMJ-43-115-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b32/9860085/70ffb77f88b7/PAMJ-43-115-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b32/9860085/728960364b31/PAMJ-43-115-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b32/9860085/c87debb10644/PAMJ-43-115-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b32/9860085/b0164d58c2da/PAMJ-43-115-g004.jpg

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Sneddon-Wilkinson Disease and Monoclonal Gammopathy of Undetermined Significance in the Elderly: Case Report.老年人的斯内登-威尔金森病与意义未明的单克隆丙种球蛋白病：病例报告
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本文引用的文献

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Subcorneal Pustular Dermatosis: A Review of 30 Years of Progress.角层下脓疱性皮肤病：30年进展回顾
Am J Clin Dermatol. 2016 Dec;17(6):653-671. doi: 10.1007/s40257-016-0202-8.
2
[Sneddon-Wilkinson disease: efficacy of intermittent adalimumab therapy after lost response to infliximab and etanercept].[斯内登-威尔金森病：英夫利昔单抗和依那西普治疗反应丧失后间歇性阿达木单抗治疗的疗效]
Ann Dermatol Venereol. 2013 Dec;140(12):797-800. doi: 10.1016/j.annder.2013.07.012. Epub 2013 Aug 13.
3
[Sneddon-Wilkinson disease. Four cases report].[斯内登-威尔金森病。4例报告]
Rev Med Interne. 2004 Feb;25(2):154-9. doi: 10.1016/j.revmed.2003.10.014.