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一名骨髓增生异常综合征患者中,7号染色体单体先于急性粒单核细胞白血病出现单核细胞受累情况。

Monocytic involvement by monosomy 7 preceded acute myelomonocytic leukemia in a patient with myelodysplastic syndrome.

作者信息

Kere J, Knuutila S, Ruutu T, Leskinen R, de la Chapelle A

机构信息

Department of Medical Genetics, University of Helsinki, Finland.

出版信息

Leukemia. 1988 Feb;2(2):69-73.

PMID:3422700
Abstract

Novel techniques were used to detect which cell lineages were affected by monosomy 7 in a patient who had myelodysplastic syndrome and later developed acute leukemia. The patient had had paroxysmal nocturnal hemoglobinuria for 20 years before developing refractory anemia with excess of blasts. Cytogenetic analysis at the myelodysplastic stage disclosed monosomy 7 in bone marrow mitoses. Restriction fragment length polymorphism analysis of fractionated white blood cells with the chromosome 7-specific probes MetH and MetD revealed that blood monocytes and most bone marrow erythroblasts but not blood granulocytes or lymphocytes were affected by monosomy 7. The patient later developed acute myelomonocytic leukemia with blast cells positive for markers of the myelomonocytic lineage but negative for granulocytic markers in a standard surface marker analysis. The leukemic blast cells had monosomy 7 as determined by direct cytogenetic investigation. Thus, the monocytes were found to be affected by monosomy 7 in this patient 8 months before her myelodysplastic syndrome progressed to acute myelomonocytic leukemia, and the affected cells had the same biologic markers at both stages of the disease.

摘要

采用新技术检测一名患有骨髓增生异常综合征并随后发展为急性白血病的患者中,哪些细胞谱系受到了7号染色体单体的影响。该患者在发展为伴有过多原始细胞的难治性贫血之前,已患有阵发性夜间血红蛋白尿20年。骨髓增生异常阶段的细胞遗传学分析显示骨髓有丝分裂中存在7号染色体单体。用7号染色体特异性探针MetH和MetD对分离的白细胞进行限制性片段长度多态性分析发现,血液单核细胞和大多数骨髓成红细胞受到7号染色体单体的影响,但血液粒细胞或淋巴细胞未受影响。该患者后来发展为急性粒单核细胞白血病,在标准表面标志物分析中,原始细胞对粒单核细胞谱系标志物呈阳性,但对粒细胞标志物呈阴性。通过直接细胞遗传学研究确定,白血病原始细胞存在7号染色体单体。因此,在该患者的骨髓增生异常综合征进展为急性粒单核细胞白血病前8个月,发现单核细胞受到7号染色体单体的影响,并且在疾病的两个阶段,受影响的细胞具有相同的生物学标志物。

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[Bone marrow monosomy 7 in children].[儿童骨髓单体7]
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