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伴有髓外肿块疾病和 22 号染色体(EWSR1)重排的前 B 细胞急性淋巴细胞白血病,表现为尤因肉瘤。

Pre-B-cell acute lymphoblastic leukemia with bulk extramedullary disease and chromosome 22 (EWSR1) rearrangement masquerading as Ewing sarcoma.

机构信息

Department of Hematology and Oncology, Pediatric Clinic, Children's Hospital Zagreb, Zagreb, Croatia.

出版信息

Pediatr Blood Cancer. 2010 Apr;54(4):606-9. doi: 10.1002/pbc.22365.

Abstract

We report a 2-year-old female with a subcutaneous tumor who was initially misdiagnosed as suffering from Ewing sarcoma with a positive EWSR1 rearrangement and EWS/FLI1 transcript. After finding lymphoblasts in peripheral blood, the diagnosis of acute lymphoblastic leukemia was established. This necessitated further analysis of the subcutaneous tumor. The tissue was positive for immature B-cell markers and an immunoglobulin heavy chain gene rearrangement, which confirmed the final diagnosis of common type acute lymphoblastic leukemia with bulk extramedullary disease. The patient was treated with chemotherapy and was in remission 30 months after the diagnosis.

摘要

我们报告了一例 2 岁女性皮下肿瘤患者,最初被误诊为 Ewing 肉瘤,具有 EWSR1 重排和 EWS/FLI1 转录本阳性。在外周血中发现淋巴母细胞后,诊断为急性淋巴细胞白血病。这需要进一步分析皮下肿瘤。组织呈幼稚 B 细胞标志物阳性和免疫球蛋白重链基因重排阳性,最终确诊为伴有髓外肿块的普通型急性淋巴细胞白血病。患者接受了化疗,在诊断后 30 个月时处于缓解状态。

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