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伴假癌样增生的Sweet综合征:一例报告并文献复习

Sweet syndrome with pseudocarcinomatous hyperplasia: A case report and review of the literature.

作者信息

Wipf Angela, Wipf Heidi, Miller Daniel

机构信息

Department of Dermatology, University of Minnesota, Minneapolis, Minnesota.

出版信息

J Cutan Pathol. 2019 Jul;46(7):520-527. doi: 10.1111/cup.13436. Epub 2019 Apr 17.

Abstract

Pseudocarcinomatous (pseudoepitheliomatous) hyperplasia represents reactive epidermal change mimicking squamous cell carcinoma (SCC), owing to a variety of inflammatory and neoplastic phenomena, including deep fungal infections, CD30-positive lymphomas, and others. We report a case of Sweet syndrome (SS) arising in a patient with acute myelogenous leukemia, with persistent orolabial involvement which mimicked SCC both clinically and microscopically, but resolved entirely with adequate corticosteroid treatment. Clinicians should be aware that neutrophilic dermatoses such as SS and pyoderma gangrenosum may rarely exhibit pseudocarcinomatous epidermal changes similar to those seen in soft tissue infections and other inflammatory dermatoses.

摘要

假癌性(假上皮瘤样)增生是一种反应性表皮改变,因包括深部真菌感染、CD30阳性淋巴瘤等多种炎症和肿瘤性现象而酷似鳞状细胞癌(SCC)。我们报告1例急性髓性白血病患者发生的Sweet综合征(SS),其口唇部持续受累,在临床和显微镜下均酷似SCC,但经适当的皮质类固醇治疗后完全消退。临床医生应意识到,SS和坏疽性脓皮病等嗜中性皮病可能很少表现出类似于软组织感染和其他炎症性皮肤病中所见的假癌性表皮改变。

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