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[慢性髓性白血病的嗜碱性粒细胞原始细胞危象]

[Basophilic blast crisis in chronic myeloid leukemia].

作者信息

García Fernández J R, montalbán M A, Martín M L, Ortiz M C, Martínez M A, García Marcilla A

机构信息

Unidad de Hematología, Hospital General Básico, Baza, Granada.

出版信息

Sangre (Barc). 1998 Oct;43(5):430-2.

PMID:9868337
Abstract

Acute basophilic leukaemia is usually characterized by a very rapid clinical course, hyperhistaminemia, resistance to antineoplastic therapy and early death due to complications related to disease. This entity is a rare condition, accounting for less than two percent of all haematopoietic malignancies. Most of the case reports are basophilic blast crisis in patients with a previous lympho or myeloproliferative disorder. A 62-year-old woman who was diagnosed as Philadelphia positive chronic myelogenous leukaemia after four years of evolution developed a basophilic blast crisis, whose characteristics are reported. Accompanying this transformation there was also a cytogenetic change. Despite chemotherapy the patient died of disease progression.

摘要

急性嗜碱性粒细胞白血病通常具有临床病程极快、高组胺血症、对抗肿瘤治疗耐药以及因疾病相关并发症导致早期死亡等特点。这种疾病较为罕见,在所有造血系统恶性肿瘤中占比不到2%。大多数病例报告是先前患有淋巴细胞或骨髓增殖性疾病的患者发生嗜碱性粒细胞母细胞危象。一名62岁女性在病程四年后被诊断为费城染色体阳性慢性粒细胞白血病,随后发生了嗜碱性粒细胞母细胞危象,本文报告了其特征。伴随这种转变还出现了细胞遗传学变化。尽管进行了化疗,患者仍因疾病进展而死亡。

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