一例原发性皮肤放线菌病。

A case of primary cutaneous actinomycosis.

作者信息

Wee S H, Chang S N, Shim J Y, Chun S I, Park W H

机构信息

Department of Dermatology, College of Medicine Pochon CHA University, Korea.

出版信息

J Dermatol. 2000 Oct;27(10):651-4. doi: 10.1111/j.1346-8138.2000.tb02247.x.

DOI:10.1111/j.1346-8138.2000.tb02247.x

PMID:11092269

Abstract

Primary cutaneous actinomycosis is very uncommon because of the exclusively endogenous habitat of the organism. We report a case of primary cutaneous actinomycosis characterized by histopathological "sulfur granules". The patient had a well-defined subcutaneous nodule on the left thigh without any other lesion and was treated with surgical excision and subsequent oral ampicillin for six weeks. There has been no recurrence during a 1-year period of follow-up.

摘要

由于放线菌的栖息地完全是内源性的，原发性皮肤放线菌病非常罕见。我们报告一例以组织病理学“硫磺颗粒”为特征的原发性皮肤放线菌病。患者左大腿有一个边界清晰的皮下结节，无其他病变，接受了手术切除，随后口服氨苄西林六周。在1年的随访期间未复发。