Osone Shinya, Hosoi Hajime, Tanaka Kazushi, Tsuchiya Kunihiko, Iehara Tomoko, Morimoto Akira, Hashida Tetsuo, Yamashita Masuo, Kawabata Kenji, Nishijo Koichi, Toguchida Junya, Hata Jun-Ichi, Sugimoto Tohru
Department of Pediatrics, Kyoto Prefectural University of Medicine, Kyoto, Japan.
J Pediatr Hematol Oncol. 2007 Dec;29(12):841-4. doi: 10.1097/MPH.0b013e318158155b.
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.
我们报告了首例在急性淋巴细胞白血病化疗3年后发生于膀胱的尤因肉瘤家族性肿瘤。一名16岁男孩在急性淋巴细胞白血病治疗后的随访期间出现肉眼血尿和排尿困难。超声检查和计算机断层扫描显示膀胱内有一个1厘米大小的肿瘤。经尿道切除肿瘤,切缘无残留肿瘤。组织病理学分析显示为小圆形蓝细胞肿瘤,CD99抗体染色阳性。通过逆转录聚合酶链反应在肿瘤组织中检测到EWS-FLI1融合转录本。这些发现支持尤因肉瘤家族性肿瘤的诊断。辅助多药化疗后,患者已无疾病证据超过2年。