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遗传性出血性毛细血管扩张症的中枢神经系统表现

CNS manifestations of hereditary hemorrhagic telangiectasia.

作者信息

Sobel D, Norman D

出版信息

AJNR Am J Neuroradiol. 1984 Sep-Oct;5(5):569-73.

PMID:6435422
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8335135/
Abstract

Hereditary hemorrhagic telangiectasia (HHT) is a familial angiodysplastic disorder. Dermal, mucosal, and visceral vascular lesions of this disorder are well known. However, central nervous system (CNS) manifestations, occurring in as many as one-third of patients, have not been well appreciated until recently. The etiology of neurologic symptomatology includes hypoxemia or ischemia secondary to pulmonary arteriovenous shunting, vascular lesions of the brain and spinal cord ranging from aneurysms to arteriovenous malformations, brain abscesses secondary to pulmonary arteriovenous fistulas, and portal systemic encephalopathy. Angiographic and computed tomographic findings in four patients with CNS involvement in HHT are reported.

摘要

遗传性出血性毛细血管扩张症(HHT)是一种家族性血管发育异常疾病。该疾病的皮肤、黏膜和内脏血管病变广为人知。然而,中枢神经系统(CNS)表现,在多达三分之一的患者中出现,直到最近才得到充分认识。神经症状的病因包括继发于肺动静脉分流的低氧血症或缺血、从动脉瘤到动静脉畸形的脑和脊髓血管病变、肺动静脉瘘继发的脑脓肿以及门体性脑病。本文报道了4例HHT合并CNS受累患者的血管造影和计算机断层扫描结果。