Yadav Y R, Rahman H H, Tandan J K, Singh B P, Kriplani T C, Mahendra R
Government Medical College, Department of Neurosurgery, Jabalpur.
J Indian Med Assoc. 2001 Feb;99(2):102-3, 110.
Primary ectopic meningiomas are rare. A case of a 16-year-old male who presented with a large mass in temporofrontal region is reported. X-ray skull showed soft tissue shadow with hyperostosis of frontal and temporal bone. CT scan of brain demonstrated a markedly enhancing lesion and bony hyperostosis with no intracranial component. Total excision of tumour with hyperostotic bone was done. Patient is well without any evidence of recurrence two years after surgery. Relevant literature is reviewed.
原发性异位脑膜瘤很罕见。本文报道了一例16岁男性患者,其颞额部出现一个巨大肿块。头颅X线显示软组织阴影,额骨和颞骨骨质增生。脑部CT扫描显示一个明显强化的病变以及骨质增生,无颅内成分。对肿瘤及增生骨质进行了全切。患者术后两年情况良好,无复发迹象。并对相关文献进行了综述。