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Langerhans cell histiocytosis of the clivus: An unusual cause of a destructive central skull base mass in a child

机译:锁骨的朗格汉斯细胞组织细胞增生:儿童中枢性颅底破坏性破坏的不寻常原因

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摘要

A 25-year-old man presented with a history of occipital headache of 6 weeks duration and a single seizure 4 weeks before admission. He had no neurologic deficit or neurocutaneous markers. Computed tomography (CT) of brain revealed a cystic lesion with a mural nodule in the right parieto-occipital lobe [Figure la and b]. Magnetic resonance imaging (MRI) showed a well-defined cystic lesion (5.7 x 3.4cm) with a solid mural nodule lateral to the occipital horn of right lateral ventricle. [Figure lc andd]. The provisional diagnosis was pilocytic astrocytoma or pleomorphic xanthoastrocytoma. He underwent right parieto-occipital craniotomy and excision of the tumor through transcortical trans-sulcal approach.
机译:一名25岁男子在入院前4星期出现枕部头痛病史,持续时间为6周,一次发作。他没有神经系统缺陷或神经皮肤标记。脑部计算机断层扫描(CT)显示右侧顶枕叶有囊性结节伴有壁结节[图1a和b]。磁共振成像(MRI)显示明确的囊性病变(5.7 x 3.4cm),右侧心室枕骨外侧有坚固的壁瘤。 [图1c和d]。临时诊断为毛细胞星形细胞瘤或多形性黄色星形细胞瘤。他进行了右顶枕开颅手术,并通过经皮穿刺的方法切除了肿瘤。

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