Yoshihara Hiroki, Yoshimoto Yuri, Hosoya Yosuke, Hasegawa Daisuke, Kawano Takafumi, Sakoda Akiko, Okita Hajime, Manabe Atsushi
Department of Pediatrics, St Luke's International Hospital, Tokyo, Japan.
Department of Pediatric Surgery, St Luke's International Hospital, Tokyo, Japan.
Pediatr Int. 2017 Mar;59(3):371-374. doi: 10.1111/ped.13229.
Infantile fibrosarcoma is a non-rhabdomyosarcoma soft-tissue sarcoma that occurs in infancy and which has a relatively good prognosis. A vincristine and dactinomycin (VA) regimen has been shown to be effective, although the duration of chemotherapy has not been well defined. We describe the case of a 4-month-old boy with a mass at the left dorsum of the foot who was diagnosed with infantile fibrosarcoma after resection of the tumor, the margin of which was macroscopically positive. VA treatment was carried out with careful monitoring of response and adverse effects. Pancytopenia was seen during the second cycle, and therapy was reduced thereafter. The treatment was continued for 38 weeks (12 cycles). There was no functional impairment, and no evidence of recurrence at 18 months after therapy.
婴儿纤维肉瘤是一种非横纹肌肉瘤的软组织肉瘤,发生于婴儿期,预后相对较好。虽然化疗疗程尚未明确界定,但长春新碱和放线菌素(VA)方案已被证明是有效的。我们描述了一名4个月大男孩的病例,他的左脚背有一个肿块,肿瘤切除后被诊断为婴儿纤维肉瘤,肿瘤边缘肉眼可见阳性。在仔细监测反应和不良反应的情况下进行了VA治疗。在第二个周期出现了全血细胞减少,此后减少了治疗剂量。治疗持续了38周(12个周期)。治疗后18个月没有功能障碍,也没有复发迹象。