Estrela F, Pinto G M, Pinto L M, Afonso A
Department of Dermatology, Curry Cabral Hospital, Lisboa, Portugal.
Cutis. 1995 Apr;55(4):233-6.
A 65-year-old white man presented with all the clinical features of acrokeratosis paraneoplastica of Bazex, characterized by violaceous erythema and scaling of the nose, aural helices, fingers, and toes, with keratoderma and severe nail dystrophy. Examination of the patient for possible associated malignancy disclosed an asymptomatic squamous cell carcinoma at the oropharyngeal region. The skin lesions resolved almost completely following radiation therapy of the neoplasm, but the onychodystrophy persisted. This case report illustrates the importance of early recognition of Bazex syndrome.
一名65岁的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，其特点为鼻子、耳廓、手指和脚趾出现紫红斑和鳞屑，伴有掌跖角化病和严重的甲营养不良。对该患者进行可能相关恶性肿瘤的检查时，发现口咽区域有一无症状的鳞状细胞癌。肿瘤接受放射治疗后，皮肤病变几乎完全消退，但甲营养不良仍然存在。本病例报告说明了早期识别巴泽克斯综合征的重要性。
