Yeo Jared J Y, Chang Kenneth T E, Ng Lee Ping, Seow Wan Tew, Low David C Y, Low Sharon Y Y
National Neuroscience Institute, Jalan Tan Tock Seng, Singapore, Singapore.
National Neuroscience Institute, Jalan Tan Tock Seng, Singapore, Singapore.
World Neurosurg. 2018 Mar;111:255-257. doi: 10.1016/j.wneu.2017.12.106. Epub 2017 Dec 26.
Cystic cerebral cavernomas belong to a rare subset of cavernous malformations in the brain. At present, there is limited information with regard to the demographics and etiology of this condition.
The authors present a case of a previously well 13-year-old male who presented with symptoms secondary to a cystic lesion of the fourth ventricle compressing on his brainstem. He underwent stereotactic aspiration of the cystic lesion and insertion of an Ommaya reservoir in the same setting. Postoperatively, his symptoms improved. The cyst fluid did not yield any positive cytology or culture results. A repeat MRI brain did not demonstrate evidence of any underlying lesion. However, the patient was readmitted for hemorrhage into the region of his previous fourth ventricular lesion. Surgical evacuation of the haematoma was performed and intraoperative tissue was sent for pathological interrogation. The final histology reported a cavernoma.
This is an unusual presentation of an intracranial vascular anomaly in a pediatric patient. Key features of the case include the diagnostic dilemma and management challenges faced from a neurosurgical perspective.
脑囊性海绵状血管瘤属于脑部海绵状畸形的罕见亚型。目前,关于该病症的人口统计学和病因学信息有限。
作者报告了一例此前健康的13岁男性病例,该患者因第四脑室囊性病变压迫脑干而出现症状。他在同一情况下接受了囊性病变的立体定向抽吸并置入了Ommaya储液囊。术后,他的症状有所改善。囊液的细胞学检查和培养结果均为阴性。脑部MRI复查未发现任何潜在病变的迹象。然而,患者因先前第四脑室病变部位出血再次入院。进行了血肿的手术清除,并将术中组织送去做病理检查。最终组织学报告为海绵状血管瘤。
这是一例儿科患者颅内血管异常的不寻常表现。该病例的关键特征包括从神经外科角度面临的诊断困境和管理挑战。