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先天性中性粒细胞减少症的经验教训:50年来在理解骨髓生成方面取得的进展。

Lessons from congenital neutropenia: 50 years of progress in understanding myelopoiesis.

作者信息

Berliner Nancy

机构信息

Division of Hematology, Brigham and Women's Hospital, Boston, MA, USA.

出版信息

Blood. 2008 Jun 15;111(12):5427-32. doi: 10.1182/blood-2007-10-077396.

Abstract

Severe congenital neutropenia (SCN) was first described just over 50 years ago. The progress in elucidating the clinical features and molecular pathophysiology of SCN closely parallels the progressive growth in our understanding of myelopoiesis. In this historical review, I have delineated this parallel progression in our understanding of the processes of granulocyte differentiation and the pathogenesis of congenital neutropenia. SCN is a heterogeneous disease that can serve as a model for the failure of myelopoiesis, and dissection of its pathogenesis has yielded important insights into the normal process of myeloid development.

摘要

严重先天性中性粒细胞减少症(SCN)于50多年前首次被描述。在阐明SCN的临床特征和分子病理生理学方面取得的进展,与我们对骨髓生成的认识的逐步发展密切平行。在这篇历史综述中,我描述了我们在粒细胞分化过程和先天性中性粒细胞减少症发病机制认识上的这种平行进展。SCN是一种异质性疾病,可作为骨髓生成失败的模型,对其发病机制的剖析为髓系发育的正常过程提供了重要见解。

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