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以尿崩症起病并随后出现急性颅神经综合征的结节病。病例报告。

Sarcoidosis presenting with diabetes insipidus followed by acute cranial nerve syndrome. A case report.

作者信息

Bruning P F, Koster H G, Hekster R E, Luyendijk W

出版信息

Acta Med Scand. 1979;205(5):441-4. doi: 10.1111/j.0954-6820.1979.tb06079.x.

Abstract

Diabetes insipidus in a previously healthy 16-year-old girl led to surgical exploration of a pituitary stalk intumescence detected by oxygen cisternography with the use of tomography. Biopsy of the pituitary stalk contained chronically inflamed brain tissue. Subsequent liver and bone biopsies showed characteristic granulomata, confirming the diagnosis of sarcoidosis. Subfrontal craniotomy was followed by a rapidly progressive basal meningoencephalitis with multiple cranial nerve involvement. The need to establish a causal diagnosis in diabetes insipidus is stressed. The rarity of the disorder and the presumed role of subfrontal craniotomy with regard to the flare-up of the sarcoidosis of the brain are discussed.

摘要

一名先前健康的16岁女孩患尿崩症,通过使用断层扫描的脑池氧气造影术检测到垂体柄肿大,遂进行手术探查。垂体柄活检发现慢性炎症的脑组织。随后的肝脏和骨骼活检显示特征性肉芽肿,确诊为结节病。额下开颅术后出现快速进展的基底脑膜脑炎,并累及多条颅神经。强调了在尿崩症中建立病因诊断的必要性。讨论了该疾病的罕见性以及额下开颅术对脑部结节病发作的推测作用。

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