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首页> 外文期刊>Journal of pediatric hematology/oncology: Official journal of the American Society of Pediatric Hematology/Oncology >A case of a ewing sarcoma family tumor in the urinary bladder after treatment for acute lymphoblastic leukemia.
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A case of a ewing sarcoma family tumor in the urinary bladder after treatment for acute lymphoblastic leukemia.

机译:一例急性淋巴细胞白血病治疗后在膀胱中出现的尤因肉瘤家族肿瘤。

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摘要

We report the first case of a tumor of the Ewing sarcoma family of tumors arising from the urinary bladder 3 years after chemotherapy for acute lymphoblastic leukemia. A 16-year-old boy complained of macrohematuria and dysuria during the posttreatment follow up of his acute lymphoblastic leukemia. Ultrasonography and computed tomography revealed a 1-cm sized intravesical tumor. The tumor was transurethrally resected with no residual tumor at the margin. Histopathologic analyses revealed a small round blue cell tumor with positive staining for CD99 antibody. EWS-FLI1 fusion transcripts were detected in the tumor tissue by reverse transcriptase polymerase chain reaction. These findings support the diagnosis of Ewing sarcoma family of tumor. After adjuvant multidrug chemotherapy, the patient has shown no evidence of disease for more than 2 years.
机译:我们报告了在急性淋巴细胞白血病化疗后3年因膀胱引起的尤因肉瘤家族肿瘤的第一例病例。一名16岁男孩在急性淋巴细胞白血病后治疗期间抱怨宏大血尿和排尿困难。超声检查和计算机断层扫描显示1cm大小的膀胱内肿瘤。经尿道切除肿瘤,边缘无残留肿瘤。组织病理学分析显示,CD99抗体呈阳性染色的小圆形蓝细胞肿瘤。通过逆转录酶聚合酶链反应在肿瘤组织中检测到EWS-FLI1融合转录物。这些发现支持尤因肉瘤家族的诊断。辅助多药化疗后,患者已超过2年未显示出疾病迹象。

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