Sakamoto Hiroki, Tanaka Toshihide, Kato Naoki, Arai Takao, Hasegawa Yuzuru, Abe Toshiaki
Department of Neurosurgery, Jikei University School of Medicine Kashiwa Hospital, Kashiwa, Chiba, Japan.
Neurol Med Chir (Tokyo). 2011;51(8):600-3. doi: 10.2176/nmc.51.600.
A 70-year-old man presented with a rare case of paranasal osteoma with secondary mucocele extending intracranially, manifesting as a generalized convulsion. Computed tomography showed a large calcified tumor adjacent to the cystic mass in the left frontal lobe. He underwent left frontal craniotomy, and the cystic lesion was totally removed. Histological examination confirmed the diagnosis of osteoma and mucocele. The giant paranasal sinus osteoma prevented growth of the mucocele into orbital recess and extension into the orbital space and paranasal sinus. The mucocele disrupted the dura in the anterior cranial fossa, resulting in a giant cystic intracranial lesion. Frontal osteoplastic craniotomy was effective for exposing both lesions and plastic repair of the dural perforation to prevent cerebrospinal fluid leakage and secondary infection.
一名70岁男性患者,出现罕见的鼻窦骨瘤合并继发性黏液囊肿并向颅内延伸的病例,表现为全身性惊厥。计算机断层扫描显示左额叶有一个与囊性肿块相邻的大钙化肿瘤。他接受了左额叶开颅手术,囊性病变被完全切除。组织学检查证实为骨瘤和黏液囊肿。巨大的鼻窦骨瘤阻止了黏液囊肿向眶隐窝生长并延伸至眶腔和鼻窦。黏液囊肿破坏了前颅窝的硬脑膜,导致巨大的颅内囊性病变。额骨成形性开颅术对于暴露两个病变以及对硬脑膜穿孔进行整形修复以防止脑脊液漏和继发感染是有效的。