Aricò M, Raiteri E, Bossi G, Giordana M T, Corbella F, Locatelli D, Pezzotta S
Department of Pediatrics, University of Pavia, IRCCS Policlinico S. Matteo, Italy.
Med Pediatr Oncol. 1994;22(4):274-8. doi: 10.1002/mpo.2950220412.
Choroid plexus carcinoma (CPC) is a rare tumor with usually severe prognosis, whose optimal treatment has not yet been established. The exact role of complete surgical resection, chemotherapy, and radiotherapy has been debated but not clarified. We report one girl with CPC diagnosed at age 3 months and apparently cured with minimal surgical resection, chemotherapy, and delayed irradiation. At the age of 8 years, she is well, with minor psychomotor retardation and growth hormone deficiency as the only sequelae.
脉络丛癌(CPC)是一种罕见肿瘤,预后通常很差,其最佳治疗方案尚未确立。手术全切、化疗及放疗的确切作用一直存在争议且尚无定论。我们报告一名3个月大时被诊断为脉络丛癌的女孩,经最小限度手术切除、化疗及延迟放疗后明显治愈。8岁时,她情况良好,仅有轻微精神运动发育迟缓及生长激素缺乏这两个后遗症。