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与慢性自然杀伤细胞淋巴细胞增多症相关的骨髓肉芽肿

Bone marrow granulomas associated with chronic natural killer cell lymphocytosis.

作者信息

Tefferi A, Li C Y

机构信息

Division of Hematology, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.

出版信息

Am J Hematol. 1997 Mar;54(3):258-62. doi: 10.1002/(sici)1096-8652(199703)54:3<258::aid-ajh14>3.0.co;2-9.

Abstract

Two patients with chronic natural killer cell lymphocytosis (CNKL) and associated bone marrow granulomas (BMGs) are described. The increases in the peripheral blood of both the proportion (64 and 74%) and absolute number (2,000/microL and 4,700/microL) of NK cells have persisted for more than 1 and 3 years. One patient was asymptomatic with thrombocytopenia and neutropenia, and the other presented with fever of unidentified origin, which has since responded to a nonsteroidal anti-inflammatory agent. Bone marrow examination in both patients showed loose aggregates of epithelioid histiocytes similar to the noncaseating granulomas seen in other diseases. An unusual feature, however, was the presence of many scattered, large mononuclear histiocytes that were morphologically similar to atypical megakaryocytes. Extensive clinical and laboratory studies did not reveal an established cause for the BMGs. BMGs may be associated with CNKL, with the unusual feature of scattered, atypical mononuclear histiocytes.

摘要

本文描述了两名患有慢性自然杀伤细胞淋巴细胞增多症(CNKL)及相关骨髓肉芽肿(BMG)的患者。两名患者外周血中自然杀伤细胞比例(分别为64%和74%)及绝对数量(分别为2,000/μL和4,700/μL)的增加持续超过1年和3年。一名患者无症状,但存在血小板减少和中性粒细胞减少,另一名患者表现为不明原因发热,使用非甾体抗炎药后症状缓解。两名患者的骨髓检查均显示上皮样组织细胞松散聚集,类似于其他疾病中所见的非干酪样肉芽肿。然而,一个不寻常的特征是存在许多散在的、形态上类似于非典型巨核细胞的大单核组织细胞。广泛的临床和实验室研究未发现BMG的确切病因。BMG可能与CNKL相关,其特征为散在的非典型单核组织细胞。

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