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具有不寻常组织学特征的皮肤类鼻疽病。

Cutaneous melioidosis with unusual histological features.

作者信息

Yeo B, Lee J, Alagappan U, Pan J Y

机构信息

National Skin Centre, Singapore.

出版信息

Clin Exp Dermatol. 2016 Apr;41(3):272-4. doi: 10.1111/ced.12726. Epub 2015 Aug 24.

DOI:10.1111/ced.12726
PMID:26299451
Abstract

Melioidosis is caused by the saprophytic gram-negative bacillus Burkholderia pseudomallei, and has varied presentations, with cutaneous manifestations occurring in about 13% of cases. The usual histopathological features of melioidosis are suppurative to chronic granulomatous inflammation. Recommended treatment of melioidosis is sequential use of intravenous followed by oral antibiotics for a few months, although oral antibiotics alone can be used in primary cutaneous melioidosis. We report a case of cutaneous melioidosis in a healthy young man, with the unusual histopathological feature of lymphoplasmacytic inflammation, and failing an initial trial of oral antibiotics alone.

摘要

类鼻疽是由腐生革兰氏阴性杆菌伯克霍尔德菌引起的,其表现多样,约13%的病例会出现皮肤表现。类鼻疽通常的组织病理学特征是化脓性至慢性肉芽肿性炎症。类鼻疽的推荐治疗方法是先静脉使用抗生素,随后口服抗生素,持续数月,不过原发性皮肤类鼻疽也可单独使用口服抗生素。我们报告了一例健康年轻男性的皮肤类鼻疽病例,其具有不寻常的淋巴浆细胞性炎症组织病理学特征,且单独口服抗生素的初始试验失败。

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Cutaneous melioidosis with unusual histological features.具有不寻常组织学特征的皮肤类鼻疽病。
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Cutaneous melioidosis in the tropical top end of Australia: a prospective study and review of the literature.澳大利亚热带北部地区的皮肤类鼻疽:一项前瞻性研究及文献综述
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Imported cutaneous melioidosis in traveler, Belgium.比利时一名旅行者的输入性皮肤类鼻疽病
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Chronic suppurative joint effusion due to burkholderia pseudomallei: a case report.由伯克霍尔德菌引起的慢性化脓性关节积液:一例报告
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Clinical features and outcome of patients with cutaneous melioidosis during a nosocomial outbreak in a temperate region of Australia.澳大利亚温带地区医院感染暴发期间皮肤类鼻疽患者的临床特征及预后
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Cutaneous melioidosis in a man who was taken as a prisoner of war by the Japanese during World War II.一名在第二次世界大战期间被日本人俘虏的男子患皮肤类鼻疽病。
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Cutaneous melioidosis and necrotizing fasciitis caused by Burkholderia pseudomallei.由类鼻疽伯克霍尔德菌引起的皮肤类鼻疽和坏死性筋膜炎。
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引用本文的文献

1
Cutaneous Melioidosis.皮肤类鼻疽
J Clin Diagn Res. 2016 Sep;10(9):WD01-WD02. doi: 10.7860/JCDR/2016/18823.8463. Epub 2016 Sep 1.