Lee Ji Yeoun, Kim Bo Sung, Phi Ji Hoon, Kang Hyoung Jin, Park Sung-Hye, Wang Kyu-Chang, Kim Il Han, Cho Byung-Kyu, Kim Seung-Ki
Division of Pediatric Neurosurgery, Cancer Research Institute, Seoul National University Children's Hospital, College of Medicine, Seoul, Republic of Korea.
J Neurosurg Pediatr. 2010 Feb;5(2):167-71. doi: 10.3171/2009.9.PEDS09256.
Primary sarcomas of the CNS are rare and are sometimes associated with chronic subdural effusion (SDE). Approximately 10 patients with such presentations have been reported. The authors report the case of a 5-year-old boy with multiple subdural masses and SDE. An SDE had been diagnosed when the patient was 2 months old, and he received a subduroperitoneal shunt when he was 5 months old. Since then, he had been clinically stable and well for 5 years. When he presented with acute headache, nausea, and vomiting, a newly developed tumor was found. Near-total resection of the tumor was performed, and the mass was diagnosed as an embryonal-type rhabdomyosarcoma. The child was given radiation therapy and 13 cycles of chemotherapy and is still free of disease 13 months after surgery.
中枢神经系统原发性肉瘤罕见,有时与慢性硬膜下积液(SDE)相关。据报道,约有10例此类病例。作者报告了一名5岁男孩,患有多个硬膜下肿块和SDE。该患者2个月大时被诊断为SDE,5个月大时接受了硬膜下-腹腔分流术。从那时起,他临床稳定且状况良好达5年。当他出现急性头痛、恶心和呕吐时,发现了一个新出现的肿瘤。对肿瘤进行了近全切除,肿块被诊断为胚胎型横纹肌肉瘤。该患儿接受了放射治疗和13个周期的化疗,术后13个月仍无疾病复发。