Richard M, Giroux J M
J Am Acad Dermatol. 1987 Jan;16(1 Pt 2):178-83. doi: 10.1016/s0190-9622(87)80057-9.
A 55-year-old white man born in Canada presented with all the clinical features of acrokeratosis paraneoplastica of Bazex. He showed the characteristic violaceous erythema and scaling of the nose and face, the aural helices, and the palmoplantar regions with severe nail dystrophy. Extensive examinations failed to reveal any associated malignancy up to 5 months after the onset of the skin eruption. While the skin was improving, and although the patient was still asymptomatic except for a weight loss of 5 kg, evidence of metastatic squamous cell carcinoma of the cervical region was obtained. Only palliative treatment could be undertaken. The bizarre clinical aspects of the syndrome are reviewed.
一名出生于加拿大的55岁白人男性,表现出巴泽克斯副肿瘤性肢端角化病的所有临床特征。他的鼻子、面部、耳廓以及掌跖部位出现了特征性的紫蓝色红斑和鳞屑,伴有严重的甲营养不良。在皮疹出现后的5个月内,广泛检查均未发现任何相关恶性肿瘤。虽然皮肤状况正在改善,且除了体重减轻5千克外患者仍无症状,但随后发现了颈部转移性鳞状细胞癌的证据。仅能进行姑息治疗。本文对该综合征奇异的临床症状进行了综述。