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一种伴有骨髓嗜酸性粒细胞增多的骨髓增生异常综合征,最终发展为急性非淋巴细胞白血病,并与16号染色体异常相关。

A myelodysplastic syndrome with marrow eosinophilia terminating in acute nonlymphocytic leukemia, associated with an abnormal chromosome 16.

作者信息

Abbondanzo S L, Gray R G, Whang-Peng J, Jacobson R J

出版信息

Arch Pathol Lab Med. 1987 Apr;111(4):330-2.

PMID:3469939
Abstract

A patient presented with a myelodysplastic syndrome and bone marrow eosinophilia that evolved six months later into an acute nonlymphocytic leukemia (ANLL). Cytogenetic analyses of the bone marrow revealed 86% of the metaphases with 45,X-Y,inv(16)(p13;q22),t(11;17) (q11;q25),del(21)(q13) and 14% of the metaphases with the same abnormalities but with a Y chromosome. The association of ANLL, bone marrow eosinophilia, and abnormal chromosome 16 has previously been reported and has been suggested to have a favorable prognosis. Our patient is unique in that ANLL was preceded by a preleukemic phase associated with bone marrow eosinophilia. When complete remission was achieved, the bone marrow cytogenetics returned to normal, and the eosinophilia disappeared.

摘要

一名患者最初表现为骨髓增生异常综合征和骨髓嗜酸性粒细胞增多,6个月后进展为急性非淋巴细胞白血病(ANLL)。对其骨髓进行的细胞遗传学分析显示,86%的中期细胞具有45,X-Y,inv(16)(p13;q22),t(11;17)(q11;q25),del(21)(q13),14%的中期细胞具有相同异常但有Y染色体。ANLL、骨髓嗜酸性粒细胞增多和16号染色体异常的关联此前已有报道,且提示预后良好。我们的患者具有独特性,即ANLL之前存在与骨髓嗜酸性粒细胞增多相关的白血病前期。当实现完全缓解时,骨髓细胞遗传学恢复正常,嗜酸性粒细胞增多消失。

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