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伴有嗜酸性粒细胞增多的急性淋巴细胞白血病:1例伴有5q缺失的病例报告及文献复习

Acute lymphoblastic leukemia with hypereosinophilia: report of a case with 5q deletion and review of the literature.

作者信息

Wynn Tung T, Heerema Nyla A, Hammond Sue, Ranalli Mark, Kahwash Samir B

机构信息

Section of Hematology/Oncology, Columbus Children's Hospital, 700 Children's Drive, Columbus, OH 43205, USA.

出版信息

Pediatr Dev Pathol. 2003 Nov-Dec;6(6):558-63. doi: 10.1007/s10024-003-2019-8.

Abstract

Peripheral blood eosinophilia as a presentation of acute lymphoblastic leukemia (ALL) has only rarely been reported. The eosinophilia is thought to be a nonneoplastic reaction to the neoplastic lymphoblasts. We present the case of a 5-year-old girl who developed peripheral hypereosinophilia with no circulating blasts prior to her diagnosis of B-cell lineage ALL. Cytogenetic study showed a hyperdiploid blast population with 5q deletion. Persistent peripheral hypereosinophilia should always be fully investigated, the possibility of a malignancy including ALL needs to be excluded, even in the absence of peripheral cytopenias and circulating blasts.

摘要

外周血嗜酸性粒细胞增多作为急性淋巴细胞白血病(ALL)的一种表现仅有极少报道。嗜酸性粒细胞增多被认为是对肿瘤性淋巴母细胞的一种非肿瘤性反应。我们报告一例5岁女孩,在诊断为B细胞系ALL之前出现外周血嗜酸性粒细胞增多且无循环原始细胞。细胞遗传学研究显示为具有5q缺失的超二倍体原始细胞群。即使在没有外周血细胞减少和循环原始细胞的情况下,对于持续性外周血嗜酸性粒细胞增多也应始终进行全面检查,排除包括ALL在内的恶性肿瘤的可能性。

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