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[神经纤维瘤病合并烟雾病和梭形动脉瘤:病例报告]

[Neurofibromatosis associated with moyamoya arteriopathy and fusiform aneurysm: case report].

作者信息

Siqueira Neto J I, Silva G S, De Castro J D, Santos A C

机构信息

Departamento de Medicina Clínica da Universidade Federal do Ceará (UFC), Brasil.

出版信息

Arq Neuropsiquiatr. 1998 Dec;56(4):819-23. doi: 10.1590/s0004-282x1998000500019.

Abstract

We report a case of von Recklinghausen's disease associated with multiple intracranial arterial occlusion ("moyamoya-like") and a fusiform aneurysm. A 28 years-old man with type I neurofibromatosis presented with syncope, complex partial seizures and mental deterioration. After an acute headache episode associated with meningeal signs, drowsiness, and hemorrhagic CSF, the patient was evaluated with cranial CT scan, MRI and angiogram that revealed an obstructive arteriopathy compatible with moyamoya disease and a fusiform aneurysm in the posterior circulation. The authors discuss the clinical and radiological findings and the therapeutic decision in this case comparing with the few similar reports in the medical literature. Recognition of an underlying rare genetic disorder may be of considerable importance in young patients presenting with seizures.

摘要

我们报告一例与多发性颅内动脉闭塞(“烟雾病样”)和梭形动脉瘤相关的冯·雷克林豪森病。一名患有I型神经纤维瘤病的28岁男性出现晕厥、复杂部分性癫痫发作和精神衰退。在一次伴有脑膜刺激征、嗜睡和血性脑脊液的急性头痛发作后,对该患者进行了头颅CT扫描、MRI和血管造影检查,结果显示存在与烟雾病相符的阻塞性动脉病变以及后循环中的梭形动脉瘤。作者结合医学文献中少数类似报告,讨论了该病例的临床和影像学表现以及治疗决策。认识到潜在的罕见遗传疾病对于出现癫痫发作的年轻患者可能具有相当重要的意义。

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