Choroid plexus carcinoma: A case report

V. S. Das, V. Bhushan, Charumathy Kathireshan
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Abstract

Choroid plexus carcinoma is a rare aggressive malignant epithelial neoplasm (WHO grade III) arising from choroid plexus epithelium. It commonly occurs in children arising in lateral ventricles. This tumour has a tendency for recurrence and metastatic dissemination along cerebrospinal fluid (CSF) pathway. We report a case of 11 month old boy presenting with hydrocephalus, irritability and vomiting. Contrast enhanced computed tomography (CECT) brain and magnetic resonance imaging (MRI) brain with contrast revealed a mass lesion within right lateral ventricle and hydrocephalus. Surgical resection was done and the excised tissue was sent for cytology and histopathological examination and a diagnosis of choroid plexus carcinoma was made.
脉络膜丛癌1例
脉络膜丛癌是一种罕见的侵袭性恶性上皮肿瘤(WHO分级III级),起源于脉络膜丛上皮。它常见于儿童侧脑室。该肿瘤有复发和沿脑脊液途径转移传播的倾向。我们报告一例11个月大的男孩表现为脑积水,易怒和呕吐。对比增强计算机断层扫描(CECT)和磁共振成像(MRI)显示右侧侧脑室和脑积水内肿块病变。手术切除后送细胞学和组织病理学检查,诊断为脉络膜丛癌。
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