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大颗粒淋巴细胞白血病的临床特征、发病机制及治疗

Clinical Features, Pathogenesis, and Treatment of Large Granular Lymphocyte Leukemias.

作者信息

Oshimi Kazuo

机构信息

Department of Medicine, Kushiro Rosai Hospital, Japan.

出版信息

Intern Med. 2017;56(14):1759-1769. doi: 10.2169/internalmedicine.56.8881. Epub 2017 Jul 15.

Abstract

Large granular lymphocytes (LGLs) are large lymphocytes with azurophilic granules in their cytoplasm. LGLs are either natural killer (NK) cells or T lymphocytes. Expansions of the LGLs in the peripheral blood are seen in various conditions, including three clonal disorders: T-cell LGL (T-LGL) leukemia, chronic lymphoproliferative disorders of NK cells (CLPD-NK), and aggressive NK-cell leukemia (ANKL). However, the monoclonal and polyclonal expansion of LGLs has been associated with many other conditions. The present article describes these LGL disorders, with special emphasis on the clinical features, pathogenesis, and treatments of the three above-mentioned clonal disorders.

摘要

大颗粒淋巴细胞(LGL)是细胞质中含有嗜天青颗粒的大淋巴细胞。LGL要么是自然杀伤(NK)细胞,要么是T淋巴细胞。外周血中LGL的增多可见于多种情况,包括三种克隆性疾病:T细胞大颗粒淋巴细胞(T-LGL)白血病、NK细胞慢性淋巴细胞增殖性疾病(CLPD-NK)和侵袭性NK细胞白血病(ANKL)。然而,LGL的单克隆和多克隆增殖也与许多其他情况有关。本文描述了这些LGL疾病,特别强调上述三种克隆性疾病的临床特征、发病机制和治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a36e/5548667/45370f56d303/1349-7235-56-1759-g001.jpg

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