Karami Kristophe J, Poulik Janet, Rabah Raja, Krass Joshua, Sood Sandeep
Department of Neurosurgery, Providence Hospital and Medical Center, Michigan State University, Southfield, Michigan 48075, USA.
J Neurosurg Pediatr. 2010 Jan;5(1):104-12. doi: 10.3171/2009.8.PEDS09117.
Simultaneous primary brain tumors in pediatric patients without prior chemotherapy or radiotherapy, phacomatosis, or known familial history are a rare occurrence. The authors report the case of a 4-year-old boy with simultaneous choroid plexus carcinoma and pilocytic astrocytoma with features of oligodendroglioma. Magnetic resonance imaging studies revealed diffuse heterogeneously enhancing left intraventricular and posterior fossa tumors initially believed most consistent with multicentric choroid plexus carcinomas. A multiple staged resection was carried out for each tumor and gross-total resection was achieved. Upon gross inspection intraoperatively as well as postoperative histological analysis, 2 distinct simultaneous tumors were identified: choroid plexus carcinoma and pilocytic astrocytoma. To the authors' knowledge this is the first case report published identifying 2 distinct tumor types with similar radiological appearances in a pediatric patient with no prior history of radiotherapy, chemotherapy, or phacomatosis.
在未接受过化疗或放疗、无母斑病或已知家族病史的儿科患者中,同时发生原发性脑肿瘤的情况极为罕见。作者报告了一例4岁男孩,同时患有脉络丛癌和具有少突胶质细胞瘤特征的毛细胞型星形细胞瘤。磁共振成像研究显示,左侧脑室内和后颅窝肿瘤呈弥漫性不均匀强化,最初认为最符合多中心脉络丛癌。对每个肿瘤进行了多阶段切除,并实现了肉眼全切。术中大体检查及术后组织学分析均发现了2种不同的同时存在的肿瘤:脉络丛癌和毛细胞型星形细胞瘤。据作者所知,这是第一例发表的病例报告,该病例中的儿科患者无放疗、化疗或母斑病病史,却同时存在2种具有相似影像学表现的不同肿瘤类型。