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难治性低血糖和癫痫发作作为空蝶鞍综合征的初始表现

Refractory Hypoglycemia and Seizures as the Initial Presenting Manifestation of Empty Sella Syndrome.

作者信息

Sethuraman Vinoth K, Viswanathan Stalin, Aghoram Rajeswari

机构信息

Department of General Medicine, Indira Gandhi Medical College And Research Institute, Pondicherry, IND.

Department of Neurology, Jawahalal Institute of Postgraduate Medical Education and Research (JIPMER), Pondicherry, IND.

出版信息

Cureus. 2018 Jun 13;10(6):e2803. doi: 10.7759/cureus.2803.

Abstract

An empty sella is reported to occur in 5.5%-23.5% of the population and is usually asymptomatic. It can be associated with endocrine disturbances. We report a 48-year-old woman who presented with refractory hypoglycemia, seizures, and shock that improved with levothyroxine, hydrocortisone, and octreotide. Investigations revealed central hypothyroidism, hypoprolactinemia, low gonadotropins, normal C-peptide and a primary empty sella. Case reports of Sheehan syndrome with or without empty sella causing hypoglycemia have been reported occasionally. Our patient had never become pregnant. She had experienced premature menopause and symptoms suggestive of hypothyroidism for many years (without treatment) before her emergency department admission for altered sensorium.

摘要

据报道,空蝶鞍在人群中的发生率为5.5%-23.5%,通常无症状。它可能与内分泌紊乱有关。我们报告一名48岁女性,她出现难治性低血糖、癫痫发作和休克,使用左甲状腺素、氢化可的松和奥曲肽后症状改善。检查发现中枢性甲状腺功能减退、低催乳素血症、促性腺激素水平低、C肽正常以及原发性空蝶鞍。偶尔有关于席汉综合征伴或不伴有空蝶鞍导致低血糖的病例报告。我们的患者从未怀孕。在因意识改变入住急诊科之前,她经历过早绝经,并有多年提示甲状腺功能减退的症状(未接受治疗)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6558/6089698/9a385ce044d9/cureus-0010-00000002803-i01.jpg

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