4型三体:临床表现、血液学和生存率。介绍两个病例并回顾相关文献。

Hematologic pathology Pub Date : 1992-01-01
B Pedersen
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引用次数: 0

摘要

2例急性非淋巴细胞白血病(ANLL)和4三体是唯一的细胞遗传畸变。包括这两例,迄今为止共报道了31例这种核型。对31例病例的回顾表明,他们分为两个不同的年龄组,较年轻的组有10例患者(5-34岁),较年长的组有21例患者(50-75岁)。除4例例外,所有病例均诊断为ANLL,主要为FAB类M2和M4。在诊断时,18人有活动性感染的临床症状。20例外周血白细胞计数高于10 × 10(9)/L,但与有无感染无关。诊断后的中位生存期为17个月。独立预后因素为诊断(p = 0.01)、外周血白细胞计数(p = 0.03)和4型三体中期百分比(p = 0.04)。这两个年龄组以及在诊断时是否存在感染没有显著的预后后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Trisomy 4: clinical picture, hematology, and survival. Presentation of two cases and review of the literature.

Two patients with acute nonlymphocytic leukemia (ANLL) and trisomy 4 as the only cytogenetic aberration are presented. Including the two, a total of 31 cases with this karyotype have been described till now. A review of the 31 cases shows that they fall into two distinct age groups, a younger group of 10 patients (5-34 years) and an older group of 21 patients (50-75 years). With four exceptions the diagnosis was ANLL in all cases, mostly FAB classes M2 and M4. At the time of diagnosis 18 had clinical signs of active infection. In 20 cases the peripheral leukocyte count was above 10 x 10(9)/L but not associated with presence/absence of infection. The median survival was 17 months from diagnosis. Independent prognostic factors were diagnosis (p = 0.01), peripheral leukocyte count (p = 0.03), and percentage of metaphases with trisomy 4 (p = 0.04). The two age groups as well as presence/absence of infection at the time of diagnosis were without significant prognostic consequences.

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