Ehmann L M, Grahovac M, Kramer M, Ruzicka T, Wollenberg A
Klinik für Dermatologie und Allergologie, Ludwig-Maximilians-Universität München, Frauenlobstr. 9-11, 80337, München, Deutschland.
Hautarzt. 2012 Jun;63(6):477-9. doi: 10.1007/s00105-011-2253-3.
Acrokeratosis paraneoplastica Bazex is a rare, obligate paraneoplasia initially presenting with palmoplantar hyperkeratosis. Later stages show acral psoriasiform lesions on other parts of the body. Common associated malignancies are laryngeal cancer and other tumors of the head or neck region or neck lymph node metastases. A 49-year-old woman presented with palmoplantar hyperkeratoses for 4 months; in addition she had a squamous cell carcinoma of the larynx. We diagnosed a minor form of acrokeratosis paraneoplastica Bazex. Some authors consider this as a separate entity, but the well- known course argues against this hypothesis. We report a case and review the literature.
巴泽克斯副肿瘤性肢端角化病是一种罕见的、必然与肿瘤相关的疾病,最初表现为掌跖角化过度。后期身体其他部位会出现肢端银屑病样损害。常见的相关恶性肿瘤是喉癌及头颈部其他肿瘤或颈部淋巴结转移瘤。一名49岁女性出现掌跖角化过度4个月;此外,她患有喉鳞状细胞癌。我们诊断为巴泽克斯副肿瘤性肢端角化病的一种轻症形式。一些作者认为这是一个独立的疾病实体,但众所周知的病程与这一假说相悖。我们报告一例病例并复习相关文献。