Lam Jordan, Lee Darrin J, Oladunjoye Azeem
Neurological Surgery, University of Michigan, Ann Arbor, USA.
Neurological Surgery, University of Southern California, Los Angeles, USA.
Cureus. 2021 Jul 2;13(7):e16122. doi: 10.7759/cureus.16122. eCollection 2021 Jul.
Transethmoidal encephaloceles are rare and most commonly present at birth with congenital abnormalities, cerebrospinal fluid rhinorrhea, or visual symptoms. Here, we report the case of a 43-year-old presenting with longstanding headache, blurry vision, anosmia, and rhinorrhea. Magnetic resonance imaging confirmed a transethmoidal encephalocele. The patient underwent craniotomy for resection of the encephalocele and repair of the cribriform defect. The postoperative course was uneventful, and the patient was discharged home with the resolution of rhinorrhea and headache. This report highlights a rare case of primary transethmoidal encephalocele undiagnosed until adulthood despite longstanding symptoms and successful treatment with resolution of symptoms.
经筛窦脑膨出较为罕见,大多在出生时伴有先天性异常、脑脊液鼻漏或视觉症状。在此,我们报告一例43岁患者,其长期存在头痛、视力模糊、嗅觉丧失和鼻漏症状。磁共振成像证实为经筛窦脑膨出。该患者接受了开颅手术以切除脑膨出并修复筛板缺损。术后过程顺利,患者出院时鼻漏和头痛症状消失。本报告强调了一例罕见的原发性经筛窦脑膨出病例,尽管症状长期存在,但直到成年才得以诊断,且通过治疗症状得以成功缓解。