Hara M, Hunayama M, Aiba S, Suetake T, Watanabe M, Tanaka M, Tagami H
Department of Dermatology, Tohoku University School of Medicine, Sendai, Japan.
Br J Dermatol. 1995 Jul;133(1):121-4. doi: 10.1111/j.1365-2133.1995.tb02504.x.
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.
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。