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首页> 外文期刊>Endocrine journal >Symptomatic Rathke's Cleft Cyst Coexisting with Central Diabetes Insipidus and Hypophysitis: Case Report
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Symptomatic Rathke's Cleft Cyst Coexisting with Central Diabetes Insipidus and Hypophysitis: Case Report

机译:有症状的Rathke裂囊肿与中枢尿崩症和垂体瘤并存:病例报告

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References(20) Cited-By(33) We describe a 48-year-old female with acute onset of central diabetes insipidus followed by mild anterior pituitary dysfunction. Magnetic resonance imaging (MRI) revealed enlargement of the hypophysis-infundibulum accompanied by a cystic component. She underwent a transsphenoidal exploration of the sella turcica. Histological examination showed foreign body type xanthogranulomatous inflammation in the neurohypophysis which might have been caused by rupture of a Rathke's cleft cyst. The MRI abnormalities and anterior pituitary dysfunction improved after a short course of corticosteroid administration, but the diabetes insipidus persisted. The histological findings in this case indicated the site of RCC rupture and the direction of the progression of RCC induced neurohypophysitis and adenohypophysitis.
机译:参考文献(20)Cyd-By(33)我们描述了一名48岁女性,其先发性中枢性尿崩症伴有轻度垂体前叶功能障碍。磁共振成像(MRI)揭示了垂体-漏斗的扩大,伴有囊性成分。她对蝶鞍进行透蝶探查。组织学检查显示神经垂体异物型黄皮肉芽肿性炎症可能是由R​​athke裂隙囊肿破裂引起的。短暂服用皮质类固醇激素后,MRI异常和垂体前叶功能障碍得以改善,但尿崩症持续存在。在这种情况下的组织学发现表明RCC破裂的部位和RCC诱导的神经垂体和腺垂体的发展方向。

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