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浅表性肉芽肿性脓皮病。两例报告。

Superficial granulomatous pyoderma. A report of two cases.

作者信息

Hardwick N, Cerio R

机构信息

Department of Dermatology, Royal Liverpool University Hospital, U.K.

出版信息

Br J Dermatol. 1993 Dec;129(6):718-22. doi: 10.1111/j.1365-2133.1993.tb03339.x.

DOI:10.1111/j.1365-2133.1993.tb03339.x
PMID:8286258
Abstract

We report two cases of superficial granulomatous pyoderma (SGP). Unlike classical pyoderma gangrenosum this variant is characterized by a benign course, superficial ulceration and a granulomatous infiltrate. Although our cases share the typical features of SGP, they are noteworthy in that one had the disease for 18 years, and the other had concomitant sarcoidosis.

摘要

我们报告两例浅表性肉芽肿性脓皮病(SGP)。与经典的坏疽性脓皮病不同,这种变体的特点是病程良性、浅表溃疡和肉芽肿浸润。尽管我们的病例具有SGP的典型特征,但值得注意的是,其中一例患病18年,另一例合并结节病。

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Superficial granulomatous pyoderma of the face: a case report and review of the literature.面部浅表性肉芽肿性脓皮病:一例报告并文献复习
Eplasty. 2012;12:e56. Epub 2012 Dec 10.