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副肿瘤性肢端角化病:巴泽克斯综合征。

Acrokeratosis paraneoplastica: Bazex syndrome.

作者信息

Valdivielso M, Longo I, Suárez R, Huerta M, Lázaro P

机构信息

Hospital Gregorio Marañón, C/Doctor Esquerdo, 46, 28007 Madrid, Spain.

出版信息

J Eur Acad Dermatol Venereol. 2005 May;19(3):340-4. doi: 10.1111/j.1468-3083.2005.01083.x.

Abstract

Bazex syndrome is a paraneoplastic dermatosis characterized by acral psoriasiform lesions associated with an underlying neoplasm. We present the case of a 64-year-old patient that was diagnosed with squamous cell lung carcinoma after being evaluated for lesions compatible with paraneoplastic acrokeratosis. With a high frequency Bazex syndrome is the earliest marker of an underlying subclinical neoplasm. An early suspicion is of the outmost importance in order to perform a prompt diagnosis of an underlying malignancy. We propose a diagnostic algorithm upon suspicion of acrokeratosis paraneoplastica and review the pathogenesis of this entity.

摘要

巴泽克斯综合征是一种副肿瘤性皮肤病,其特征为肢端银屑病样皮损并伴有潜在肿瘤。我们报告一例64岁患者,该患者因评估与副肿瘤性肢端角化病相符的皮损后被诊断为肺鳞状细胞癌。巴泽克斯综合征作为潜在亚临床肿瘤的最早标志物,出现频率较高。早期怀疑对于及时诊断潜在恶性肿瘤至关重要。我们提出一种疑似副肿瘤性肢端角化病的诊断算法,并回顾该疾病实体的发病机制。

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