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患有冯·雷克林霍增氏病的儿童的非肿瘤性导水管狭窄

Nontumoral aqueductal stenosis in children affected by von Recklinghausen's disease.

作者信息

Spadaro A, Ambrosio D, Moraci A, Albanese V

出版信息

Surg Neurol. 1986 Nov;26(5):487-95. doi: 10.1016/0090-3019(86)90262-4.

Abstract

The authors report three cases of primary nontumoral aqueductal stenosis associated with von Recklinghausen's disease in children. Moreover, 16 similar cases collected from the literature are presented. The clinical features are evaluated in light of data from the literature. Among all 19 cases, the median age was 19 years (range 6-46 years), and nine patients were under the age of 13 years. Our own patients underwent ventriculoatrial shunt procedures, followed by clinical recovery (follow-up 2-5 years). In one patient, computed tomography scanning performed 20 months after the operation showed a chronic calcified subdural hematoma in the right frontoparietal area. In conclusion, it is felt that, among all the pathological events usually described in patients affected by neurofibromatosis, primary aqueductal stenosis seems to be part of the natural history of this neurological syndrome.

摘要

作者报告了3例儿童原发性非肿瘤性导水管狭窄合并冯·雷克林霍增氏病的病例。此外,还展示了从文献中收集的16例类似病例。结合文献数据对临床特征进行了评估。在所有19例病例中,中位年龄为19岁(范围6 - 46岁),9例患者年龄在13岁以下。我们自己的患者接受了脑室心房分流术,随后临床症状恢复(随访2 - 5年)。1例患者术后20个月进行的计算机断层扫描显示右侧额顶叶区域有慢性钙化性硬膜下血肿。总之,人们认为,在通常描述的神经纤维瘤病患者的所有病理事件中,原发性导水管狭窄似乎是这种神经综合征自然病程的一部分。

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