继发于垂体柄病变的神经神经官能症表现为 "阿狄森氏糖尿病",并与抗NMDA受体抗体有关。

IF 0.9 Q4 CLINICAL NEUROLOGY Case Reports in Neurological Medicine Pub Date : 2020-06-25 eCollection Date: 2020-01-01 DOI:10.1155/2020/7956350
Jose Gabriel Solis, Arturo Olascoaga Lugo, Marco Antonio Rodríguez Florido, Bayron Alexander Sandoval Bonilla, Jose Malagón Rangel
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引用次数: 0

摘要

肉样瘤病是一种病因不明的多系统炎症性疾病。其特征是活检标本上出现非溃疡性肉芽肿。不同病例的临床表现各不相同,既有发热、呼吸道症状和皮肤损害等多种症状,也有心脏传导阻滞或神经系统症状等非典型症状。因此,我们报告了一名 22 岁女性的病例,她患有脑炎、垂体肿块和腺性尿崩症。诊断方法并没有因为对病变部位进行活检(活检结果显示为非酪氨酸肉芽肿)而结束;相反,这是排除中枢神经系统肉芽肿其他病因的开始,最终诊断为孤立性中枢神经系统肉样瘤病。此外,我们还首次报告了抗NMDA受体抗体与肉样瘤病之间的关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Neurosarcoidosis Presentation as Adipsic Diabetes Insipidus Secondary to a Pituitary Stalk Lesion and Association with Anti-NMDA Receptor Antibodies.

Sarcoidosis is a multisystemic inflammatory disease of unknown cause. It is characterized by the presence of noncaseating granuloma on a biopsy specimen. Clinical presentation varies across case report series with myriad of symptoms ranging from fever, respiratory symptoms, and skin lesions, or atypical symptoms like heart block or neurological symptoms. Hence, we report the case of a 22-year-old woman with encephalitis, a pituitary mass, and adipsic diabetes insipidus. The diagnostic approach did not end on the biopsy of the lesion, which reported noncaseating granulomas; on the contrary, it was the beginning of a path to exclude other causes of the central nervous system granulomas that ended with the diagnosis of the isolated central nervous system sarcoidosis. Also, we report the first proven association between anti-NMDA receptor antibodies and sarcoidosis.

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