Mishra Ashish, Maurya Ved Prakash, Chaudhary Nandita, Srivastava Arun Kumar
Department of Neurosurgery, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Department of Pathology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Surg Neurol Int. 2025 Aug 15;16:345. doi: 10.25259/SNI_579_2025. eCollection 2025.
Sarcoidosis is an immune-mediated disorder characterized by granulomatous inflammation of the affected organ. Isolated neurosarcoidosis presents as aseptic granulomatous meningitis or focal mass lesions due to granulomas. This case is notable for its radiological resemblance to meningiomatosis, which has a substantial disease burden.
A 47-year-old man presented with symptoms of vertigo and right-sided hearing impairment for the past year. After 6 months, he experienced progressive visual impairment in the right eye and a headache associated with dural stretching on the right side. Neurological evaluation revealed significant visual impairment in the right eye, limited to finger counting at 1 m. The right-sided primary optic atrophy was due to mass effect from the sarcoid granuloma on the optic nerve. Pure-tone audiometry indicated mild sensorineural hearing loss on the right side. Radiological investigations showed multiple intracranial lesions, with the largest lesion located at the right anterior clinoid, exhibiting pial breach, and perilesional edema. The institutional tumor board diagnosed cerebral meningiomatosis. Due to rapidly progressive visual deterioration caused by the right clinoidal lesion, a right pterional craniotomy with gross total excision of the lesion was performed. The histopathology evaluation report revealed neurosarcoidosis. The patient was started on glucocorticoids and immunosuppressant medication by clinical immunology. Follow-up magnetic resonance imaging of the brain after 1 year showed stable disease without any recurrence.
Surgical removal of lesions causing mass effect should be regarded as the primary therapy. Insufficient response to medical treatment may result in permanent deficits. When dealing with multiple intracranial lesions, the aim should be to achieve optimal results through surgical intervention.
结节病是一种免疫介导的疾病,其特征为受累器官出现肉芽肿性炎症。孤立性神经结节病表现为无菌性肉芽肿性脑膜炎或因肉芽肿导致的局灶性肿块病变。该病例因其影像学表现与脑膜瘤病相似而值得关注,脑膜瘤病具有相当大的疾病负担。
一名47岁男性在过去一年中出现眩晕和右侧听力减退症状。6个月后,他右眼出现进行性视力损害,并伴有右侧硬脑膜牵拉引起的头痛。神经学评估显示右眼有明显视力损害,仅能在1米处数指。右侧原发性视神经萎缩是由于结节病肉芽肿对视神经的占位效应所致。纯音听力测定表明右侧有轻度感音神经性听力损失。影像学检查显示颅内有多个病变,最大的病变位于右侧前床突,表现为软脑膜侵犯和病变周围水肿。该机构的肿瘤委员会诊断为脑膜瘤病。由于右侧床突病变导致视力迅速恶化,遂进行了右侧翼点开颅手术,将病变大体全切。组织病理学评估报告显示为神经结节病。临床免疫学开始给予患者糖皮质激素和免疫抑制药物治疗。1年后的脑部随访磁共振成像显示病情稳定,无任何复发。
手术切除引起占位效应的病变应被视为主要治疗方法。对药物治疗反应不足可能导致永久性缺陷。在处理多个颅内病变时,目标应是通过手术干预取得最佳效果。