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白血病前期:白血病发病前的血液学紊乱。

Preleukemia: hematological disorders prior to onset of leukemia.

作者信息

Takahashi I, Nakanishi T, Sakato J, Mikochi H, Kitajima K

出版信息

Acta Med Okayama. 1975 Dec;29(6):437-44.

PMID:132844
Abstract

Published data on Japanese leukemia patients with a preleukemic hematological disorder were assessed. The reexamined cases were from the "Japona Centra Revuo Medicina" reported during the period from 1952 to 1971. Among preleukemic hematological disorders, hypoplastic anemia was the most frequently reported (41 of 62 cases). These "hypoplastic preleukemia" patients were rather elderly and terminated mostly in atypical myelocytic leukemia. The chief hematological feature of the hypoplastic preleukemia cases was the coexistence of a relative erythroid hyperplasia and a slight increase of myeloblasts in the bone marrow that was unusual in hypoplastic anemia. The presence of pancytopenia and hypocellular marrow with a relative erythroid hyperplasia combined with a slight increase of myeloblasts probably indicates hypoplastic preleukemia that terminates later in acute leukemia.

摘要

对已发表的有关患有白血病前期血液系统疾病的日本白血病患者的数据进行了评估。重新审查的病例来自1952年至1971年期间报告的《日本中央医学杂志》。在白血病前期血液系统疾病中,再生障碍性贫血是报告最为频繁的(62例中有41例)。这些“再生障碍性白血病前期”患者年龄较大,大多发展为非典型粒细胞白血病。再生障碍性白血病前期病例的主要血液学特征是骨髓中相对红系增生与原粒细胞轻度增加并存,这在再生障碍性贫血中并不常见。全血细胞减少、骨髓细胞减少伴相对红系增生以及原粒细胞轻度增加可能提示再生障碍性白血病前期,其后期会发展为急性白血病。

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