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沃林格-科洛普型亲表皮性网状细胞增生病(作者译)

[Epidermotropic reticulosis of the Woringer-Kolopp type (author's transl)].

作者信息

Bourlond A, Delbrouck-Poot F, Philippart J L, Bourlond-Reinert L

出版信息

Dermatologica. 1979;159(2):101-14.

PMID:478049
Abstract

A 46-year-old female, otherwise healthy, developed erythematous, pseudotumoral nodules, mainly on the hands; biopsies led to the diagnosis of Woringer-Kolopp disease. Anti-anergic chemotherapy with levamisole proved hazardous but, possibly, beneficial. Classification into benign localized, fatal generalized and intermediate disease is briefly commented upon. Differential diagnosis and tumor origin are discussed; while the Merkel cell hypothesis has been recently advanced strong analogies and slight discrepancies with mycosis fungoides advocate the T cell lymphoma theory.

摘要

一名46岁的健康女性手部出现了主要为红斑性假肿瘤结节;活检确诊为沃林格-科洛普病。左旋咪唑抗无反应性化疗被证明有风险,但可能有益。文中简要评论了将其分为良性局限性、致命性全身性和中间型疾病的分类方法。讨论了鉴别诊断和肿瘤起源;虽然最近有人提出默克尔细胞假说,但与蕈样肉芽肿的强烈相似性和细微差异支持T细胞淋巴瘤理论。

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