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与骨髓增生异常综合征相关的慢性嗜中性皮病中的未成熟髓样前体细胞。

Immature myeloid precursors in chronic neutrophilic dermatosis associated with myelodysplastic syndrome.

作者信息

Tomasini C, Aloi F, Osella-Abate S, Dapavo P, Pippione M

机构信息

Department of Medical and Surgical Specialties, Second Dermatologic Clinic, University of Turin, Italy.

出版信息

Am J Dermatopathol. 2000 Oct;22(5):429-33. doi: 10.1097/00000372-200010000-00008.

Abstract

Sweet syndrome (SS) associated with myeloproliferative disorders has been considered an inflammatory process mediated by neutrophils in which immunologic mechanisms are operative. The authors report the case of a 68-year-old man suffering from a myelodysplastic syndrome, who presented with a relapsing skin eruption resembling SS. Histopathologically, the skin infiltrates showed prominent neutrophilic features masking the underlying malignant process. Extensive immunophenotypic studies of skin revealed the presence of a few immature myeloid cells intermingled with an overwhelming infiltrate of neutrophils. The atypical cells in the skin had a phenotype identical to that of leukemic cells in the peripheral blood and bone marrow. Whether or not immature myeloid cell precursors constitute a specific infiltrate of leukemia cutis or are a result of recruitment of circulating leukemic cells to this area of inflammation is discussed.

摘要

与骨髓增殖性疾病相关的Sweet综合征被认为是一种由中性粒细胞介导的炎症过程,其中免疫机制起作用。作者报告了一例68岁患有骨髓增生异常综合征的男性病例,该患者出现了类似Sweet综合征的复发性皮疹。组织病理学上,皮肤浸润显示出突出的中性粒细胞特征,掩盖了潜在的恶性过程。对皮肤进行的广泛免疫表型研究显示,有一些未成熟髓样细胞与大量中性粒细胞浸润混合存在。皮肤中的非典型细胞具有与外周血和骨髓中白血病细胞相同的表型。本文讨论了未成熟髓样细胞前体是否构成皮肤白血病的特异性浸润,或者是循环白血病细胞募集到该炎症区域的结果。

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