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选择性髓系发育不全:一种不寻常的毛细胞白血病变异型的长期表现?

Selective myeloid aplasia: a long-lasting presentation of an unusual hairy cell leukemia variant?

作者信息

Marinone G M, Roncoli B

机构信息

Department of Internal Medicine, University of Pavia, Italy.

出版信息

Haematologica. 1993 Jul-Aug;78(4):239-41.

PMID:8294056
Abstract

A rare aleukemic myeloaplastic presentation of hairy cell leukemia (HCL) is described. The patient was observed for 11 years and presented a clinical picture suggestive of pure white cell aplasia for seven years. Hairy cells (HC) were first discovered in the bone marrow, then occasionally in the blood during the last four years. A brief course of low-dose alpha interferon promptly induced prolonged remission of neutropenia. In our opinion, this case, as few others described till now, should be considered a rare HCL variant, an understanding of which offers an important clinical opportunity for investigating the myeloid inhibitory activity of hairy cells.

摘要

描述了1例罕见的毛细胞白血病(HCL)的无白血病性骨髓发育不全表现。该患者被观察了11年,有7年临床表现提示为纯白细胞再生障碍。毛细胞(HC)最初在骨髓中发现,在过去4年中偶尔在血液中发现。低剂量α干扰素的一个短疗程迅速诱导了中性粒细胞减少症的长期缓解。我们认为,与迄今描述的其他少数病例一样,该病例应被视为一种罕见的HCL变异型,对其的了解为研究毛细胞的髓系抑制活性提供了重要的临床契机。

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