Kudawara Ikuo, Araki Nobuhito, Myoui Akira, Uchida Atsumasa, Fukuda Haruki, Yoshikawa Hideki
Department of Orthopaedic Surgery, Osaka National Hospital, Osaka, Japan.
Clin Orthop Relat Res. 2004 Jan(418):198-201. doi: 10.1097/00003086-200401000-00032.
A 23-year-old man had eight cycles of adjuvant chemotherapy including doxorubicin, cisplatin, methotrexate, and ifosfamide and radical surgery for biopsy-proved osteosarcoma of the right fibular shaft. Two years after the initial diagnosis, he noticed a mass in the medial aspect of his right knee. Magnetic resonance imaging scans revealed a soft tissue tumor measuring 2 x 2 cm in the pericapsular region of the right knee. Histologically, this soft tissue tumor was composed of spindle cells with occasional atypical mitoses and without matrix formation. Immunohistochemically, the tumor cells were positive for vimentin, cytokeratin, and epithelial membrane antigen, and negative for alpha smooth muscle actin. A fusion gene, SYT-SSX was detected with reverse transcription-polymerase chain reaction. From the results, the secondary tumor was diagnosed as a synovial sarcoma. The current case of double sarcomas is rare. Both sarcomas were diagnosed accurately using immunohistochemical and molecular procedures. This case suggests a positive association between a second tumor and chemotherapy including intraarterial perfusion of doxorubicin.
一名23岁男性因活检证实的右腓骨干骨肉瘤接受了8个周期的辅助化疗,化疗方案包括多柔比星、顺铂、甲氨蝶呤和异环磷酰胺,并接受了根治性手术。初次诊断两年后,他注意到右膝内侧有一个肿块。磁共振成像扫描显示右膝囊周区域有一个2×2厘米的软组织肿瘤。组织学上,这个软组织肿瘤由梭形细胞组成,偶尔有非典型有丝分裂,无基质形成。免疫组织化学检查显示,肿瘤细胞波形蛋白、细胞角蛋白和上皮膜抗原呈阳性,α平滑肌肌动蛋白呈阴性。通过逆转录聚合酶链反应检测到一个融合基因SYT-SSX。根据这些结果,继发性肿瘤被诊断为滑膜肉瘤。目前这种双肉瘤病例很罕见。两种肉瘤均通过免疫组织化学和分子检测方法准确诊断。该病例提示第二种肿瘤与包括多柔比星动脉内灌注在内的化疗之间存在正相关。