Department of Neurosurgery, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Department of Neurosurgery, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
World Neurosurg. 2022 Jun;162:74-76. doi: 10.1016/j.wneu.2022.03.068. Epub 2022 Mar 18.
Infantile choroid plexus papilloma (CPP) associated with multiple peritumoral cysts is a rare variant of CPP, and clinical course and optimal management are largely unknown. A 9-month-old boy presented with a large solid tumor in the left lateral ventricle associated with multiple peritumoral cysts, arachnoid cysts, and hydrocephalus containing xanthochromic fluid with high protein content. Shrinkage of these cysts and resolution of hydrocephalus were achieved after total resection of the hypervascular solid part of the tumor. Histological examination confirmed the solid part of the tumor as CPP and showed that the wall of the peritumoral cysts consisted of reactive gliosis without neoplastic cells. Follow-up magnetic resonance imaging 12 months after surgery revealed that these cysts remained stable. CPP with nonenhancing peritumoral cysts can be managed by resection of only the solid part of the tumor without permanent cerebrospinal fluid diversion.
婴儿型脉络丛乳头状瘤(CPP)伴多发瘤周囊肿是 CPP 的一种罕见变异,其临床病程和最佳治疗方法尚不清楚。一名 9 月龄男婴因左侧侧脑室巨大实性肿瘤就诊,伴多发瘤周囊肿、蛛网膜囊肿和含高蛋白质含量的黄变液的脑积水。肿瘤富含血管的实性部分全切术后,这些囊肿缩小,脑积水缓解。组织学检查证实实性部分为 CPP,且瘤周囊肿的壁由反应性神经胶质增生而非肿瘤细胞组成。术后 12 个月的磁共振成像随访显示这些囊肿保持稳定。无强化瘤周囊肿的 CPP 可仅切除肿瘤的实性部分,而无需永久性脑脊液分流。