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副肿瘤性肢端角化病(巴泽克斯综合征)伴小腿原发性皮肤鳞状细胞癌、白癜风和斑秃。

Acrokeratosis paraneoplastica (Bazex syndrome) associated with primary cutaneous squamous cell carcinoma of the lower leg, vitiligo and alopecia areata.

作者信息

Hara M, Hunayama M, Aiba S, Suetake T, Watanabe M, Tanaka M, Tagami H

机构信息

Department of Dermatology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Br J Dermatol. 1995 Jul;133(1):121-4. doi: 10.1111/j.1365-2133.1995.tb02504.x.

Abstract

We report a case of acrokeratosis paraneoplastica (AP; Bazex syndrome), characterized by typical palmoplantar hyperkeratosis and psoriasiform scaly erythema of the acral regions, associated with primary cutaneous squamous cell carcinoma (SCC) on the left lower leg. This 54-year-old Japanese man subsequently developed vitiligo, and alopecia areata of the scalp. Serial monitoring of squamous cell carcinoma antigen (SCC-Ag) demonstrated that the severity of the clinical manifestations of AP paralleled the serum concentrations of SCC-Ag. We suggest that an immune-mediated mechanism underlies the development of AP in this patient.

摘要

我们报告了一例副肿瘤性肢端角化病(AP;巴泽克斯综合征),其特征为典型的掌跖角化过度以及肢端部位的银屑病样鳞屑红斑,同时左小腿患有原发性皮肤鳞状细胞癌(SCC)。这位54岁的日本男性随后出现了白癜风和头皮斑秃。对鳞状细胞癌抗原(SCC-Ag)的连续监测表明,AP临床表现的严重程度与SCC-Ag的血清浓度平行。我们认为免疫介导机制是该患者发生AP的基础。

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