Gross E, Rao B N, Pappo A, Bowman L, Shearer P, Kaste S, Greenwald C, Michalkiewicz E, Pratt C
Department of Surgery, Hematology-Oncology, Diagnostic Imaging, St Jude Children's Research Hospital, Memphis, TN 38105, USA.
J Pediatr Surg. 1996 Dec;31(12):1663-5. doi: 10.1016/s0022-3468(96)90043-3.
Literature regarding the natural history and prognosis of epithelioid sarcoma in the pediatric population is sparse. During the past 11 years, eight patients with epithelioid sarcoma were treated at St Jude Children's Research Hospital. Of the eight children, six of whom were male, seven presented with localized disease and one with metastatic disease. The primary tumor was located in the upper extremity in four patients; the other sites were the scalp, external ear, back, and mediastinum. The mean duration of symptoms before diagnosis was 8.3 months (range, 1 to 12 months). Surgical treatment comprising amputation or wide local excision was performed in six patients, three of whom had additional lymph node dissection. Three patients received multiagent chemotherapy, and four patients were treated with supplementary radiation. Two patients died of progressive local and distant disease within 9 months of diagnosis. The other six patients are alive and have no evidence of disease 12 months to 10 years 6 months after the completion of treatment.
关于小儿上皮样肉瘤自然病史和预后的文献很少。在过去11年中,圣裘德儿童研究医院治疗了8例上皮样肉瘤患者。这8名儿童中,6名是男性,7例为局限性疾病,1例为转移性疾病。4例患者的原发肿瘤位于上肢;其他部位为头皮、外耳、背部和纵隔。诊断前症状的平均持续时间为8.3个月(范围为1至12个月)。6例患者接受了包括截肢或广泛局部切除在内的手术治疗,其中3例还进行了淋巴结清扫。3例患者接受了多药化疗,4例患者接受了辅助放疗。2例患者在诊断后9个月内死于局部和远处疾病进展。其他6例患者存活,在完成治疗后12个月至10年6个月内无疾病证据。