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慢性粒细胞白血病初发时的淋巴母细胞危象:两例报告。

Lymphoid blastic crisis at the onset of chronic granulocytic leukemia: report of two cases.

作者信息

Mauri C, Torelli U, di Prisco U, Silingardi V, Artusi T, Emila G

出版信息

Cancer. 1977 Aug;40(2):865-70. doi: 10.1002/1097-0142(197708)40:2<865::aid-cncr2820400240>3.0.co;2-q.

Abstract

Two patients with a typical hematologic pattern of acute lymphatic leukemia were brought into complete remission by treatment. A few weeks later they developed a typical peripheral and bone marrow pattern of chronic granulocytic leukemia, with Philadelphia chromosome and very low leukocyte alkaline phosphatase. These cases, along with other findings recently reported in the literature, support the possibility of a previously unrecognized relationship between lymphoblastic cell populations and chronic granulocytic leukemia.

摘要

两名具有典型急性淋巴细胞白血病血液学模式的患者经治疗后完全缓解。几周后,他们出现了典型的慢性粒细胞白血病外周血和骨髓模式,伴有费城染色体和极低的白细胞碱性磷酸酶。这些病例以及文献中最近报道的其他发现,支持了淋巴细胞群体与慢性粒细胞白血病之间存在以前未被认识到的关系的可能性。

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