He Zhan, Ding Fang, Rong Jiandong, Gan Yongli
Department of Neurosurgery, Lihuili Hospital of Ningbo Medical Center, Ningbo 315041, China.
Clinical Pathology Diagnosis Center, Ningbo 315031, China.
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2016 May 25;45(5):540-543. doi: 10.3785/j.issn.1008-9292.2016.09.14.
A 26-year-old male presented with a 6-day history of paroxysmal headache which was worsen with nausea and vomiting for 1 day. Head CT on admission revealed left chronic subdural hematoma with midline shift. An emergency Burr hole drainage for hematoma was performed. Headache recurred 6 days later. MRI of the brain revealed a diffuse thickening and a gadolinium-enhancement of the falx, cranial dura mater and tentorium cerebelli on the left side with pia mater involved. Lumber puncture showed increased intracranial pressure and elevated IgG level in cerebrospinal fluid. Histological examination of the biopsy specimen showed thickened, fibrotic dura with a sterile chronic inflammation. According to pathological examination, idiopathic hypertrophic cranial pachymeningitis was considered as the final diagnosis. Symptoms were improved with steroid pulse therapy.
一名26岁男性,阵发性头痛6天,伴有恶心、呕吐1天,且症状加重。入院时头部CT显示左慢性硬膜下血肿伴中线移位,遂行急诊血肿钻孔引流术。6天后头痛复发。脑部MRI显示左侧大脑镰、硬脑膜及小脑幕弥漫性增厚并钆增强,软脑膜受累。腰椎穿刺显示颅内压升高,脑脊液中IgG水平升高。活检标本的组织学检查显示硬脑膜增厚、纤维化,伴有无菌性慢性炎症。根据病理检查,最终诊断为特发性肥厚性硬脑膜炎。经类固醇脉冲治疗后症状改善。