副瘤性肢端角化病(Bazex综合征)1例报告。

IF 0.9 Q4 DERMATOLOGY
Case Reports in Dermatology Pub Date : 2022-10-20 eCollection Date: 2022-09-01 DOI:10.1159/000525381
Julia Holzgruber, Jacqueline Oberneder-Popper, Emmanuella Guenova, Wolfram Hötzenecker
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引用次数: 1

摘要

副瘤性肢端角化病是一种罕见的副瘤性皮肤表现,通常引起肢端银屑病样病变。患者通常表现为红斑性角化过度,手、脚或其他肢端部位(如耳朵或鼻子)有黄色粘附鳞片。我们在此报告一例Bazex综合征的男性患者,他以前被诊断为肝细胞癌。我们的病例报告强调了这种罕见的情况,因为早期诊断可能会影响患者的肿瘤病程和预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Acrokeratosis Paraneoplastica (Bazex Syndrome): A Case Report.

Acrokeratosis Paraneoplastica (Bazex Syndrome): A Case Report.

Acrokeratosis Paraneoplastica (Bazex Syndrome): A Case Report.

Acrokeratosis paraneoplastica Bazex is a rare paraneoplastic skin manifestation, typically causing acral psoriasiform lesions. Patients usually show erythematous hyperkeratosis with yellowish, adherent scales on the hands and feet or other acral locations such as ears or nose. We herein report a case of Bazex syndrome in a male patient, who was previously diagnosed with hepatocellular carcinoma. Our case report highlights this rare condition as early diagnosis may impact the patient's course of tumor disease and prognosis.

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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
57
审稿时长
9 weeks
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