原发性颅内横纹肌肉瘤--一例罕见病例的报告及文献综述

MA Joarder, Alam Smm, Dr. Md Aliuzzaman Joarder, Dr Asaduzzaman, Dr. Ahmed Khaled, Dr. Md. Asfaquzzaman, Dr. Nahid Akter
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引用次数: 0

摘要

一名 29 岁的男性患者出现 H/O 头痛和呕吐 4 个月,视力模糊和步态共济失调 2 个月。脑部对比 MRI 显示,病灶来自左侧小脑半球的硬脑膜。对患者进行了后窝开颅手术,初步诊断为脑膜瘤。组织病理学和免疫组化显示为雷肌瘤。包括对比 CT 和 PET 扫描在内的进一步评估未能确定任何原发部位。原发性颅内线粒体肉瘤非常罕见,以前只有少数病例报道过。原发性颅内亮肌肉瘤的预后很差,最长的存活期为 32 个月。砰J Neurosurgery 2023; 13(1):48-50
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Primary Intracranial Leiomyosarcoma- Report of a Rare Case with Literature Review
A 29 years old man presented with a H/O headache and vomiting for 4 months, blurring of vision and gait ataxia for 2 months. A contrast MRI of brain indicated the lesion arose from the dura over left cerebellar hemisphere. A posterior fossa craniotomy was performed with a provisional diagnosis of meningioma. Histopathology and immunohistochemistry revealed Leiomyosarcoma. Further evaluation including Contrast CT and PET scan failed to identify any primary site. Primary intracranial leiomyosarcoma is very rare and only few cases were previously reported. The prognosis for primary intracranial leiomyosarcoma is poor with the longest reported survival being 32 months. Bang. J Neurosurgery 2023; 13(1): 48-50
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