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大颗粒性淋巴细胞白血病相关的纯红细胞发育不良的病理生理机制和处理
Authors Qiu ZY, Qin R, Tian GY, Wang Y, Zhang YQ
Received 8 July 2019
Accepted for publication 13 September 2019
Published 4 October 2019 Volume 2019:12 Pages 8229—8240
DOI https://doi.org/10.2147/OTT.S222378
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Ms Aruna Narula
Peer reviewer comments 3
Editor who approved publication: Dr Arseniy Yuzhalin
Abstract: Large granular lymphocytic leukemia (LGLL) is a chronic clonal lymphoproliferative disease of mature T or NK cells, and produces a variety of hematological abnormalities. Pure red cell aplasia (PRCA) is a rare haematological disease and is one of the most common complications of LGLL. LGLL-associated PRCA may represent a relatively indolent type and may be more common than reported, but its natural history and clinical course have not been well described. The ethnic origin of the patients is an important consideration in determining the relationship between PRCA and LGLL. Guidelines and progresses for management of LGLL-associated PRCA rely on accumulation of empirical experiences, integrative analyses of several cases and clinical trials. The purpose of this review is to evaluate occurrence, possible mechanisms, diagnosis, clinical features, treatments and outcomes of LGLL-associated PRCA.
Keywords: large granular lymphocytic leukemia, lymphocytosis, PRCA
