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t(8;21) (q22;q22) acute myelogenous leukemia in Mexico: a single institution experience.

机译:墨西哥的t(8; 21)(q22; q22)急性骨髓性白血病:单一机构经验。

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摘要

We analyze the prevalence and clinical features of a group of patients with t(8;21) (q22;q22) acute myeloblastic leukemia, identified in a single institution in Mexico over a 10-year period. Fifteen patients presented at the Centro de Hematologia y Medicina Interna de Puebla from February 1995 to August 2005; only nine were treated and followed in the institution. Median age was 24 years, (range 7-49); there was only one male. According to the French-American-British (FAB) morphological classification of leukemia, the morphology was M2 in four cases, M4 in three cases, M3 in one case and M0 in one. In addition to the myeloid markers, lymphoid markers were identified in 6 patients. Patients were induced to remission with combined chemotherapy and three subsequently underwent bone marrow transplantation (BMT). The median overall and disease-free survival has not been reached, being above 3390 days, the probability of survival at this time was 73%. In this single-center experience in Mexico, we found thatthe t(8;21) (q22;q22) variant of leukemia was more frequent than in Caucasian populations, that the co-expression of lymphoid markers in the blast cells is very frequent and that this malignancy is associated with a relatively good prognosis.
机译:我们分析了一组在墨西哥的单一机构在十年内发现的t(8; 21)(q22; q22)急性粒细胞白血病患者的患病率和临床特征。 1995年2月至2005年8月,在普埃布拉国际血液中心和地中海医学中心就诊的患者有15例;在该机构中只有9人得到治疗和随访。中位年龄为24岁(范围7-49);只有一名男性。根据法国-美国-英国(FAB)白血病的形态学分类,形态为M2 4例,M4 3例,M3 1例和M0 1。除了骨髓标记物外,在6例患者中还发现了淋巴样标记物。联合化疗使患者缓解,随后三例接受了骨髓移植(BMT)。尚未达到3390天以上的总体中位数和无病生存时间,此时生存的可能性为73%。在墨西哥的这一单中心经验中,我们发现白血病的t(8; 21)(q22; q22)变异比高加索人群更常见,在胚细胞中淋巴标记物的共表达非常频繁,并且该恶性肿瘤预后相对较好。

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