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Lymphocytic hypophysitis in the elderly

机译:老年人淋巴细胞性垂体炎

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摘要

We report a 73-year-old woman with lymphocytic hypophysitis who presented with atypical clinical features and what appeared to be pituitary apoplexy on radiological analysis. Lymphocytic hypophysitis is a rare cause of pituitary dysfunction, and is thought to be an autoimmune disorder. It typically affects young peri-partum women, with clinical features that are related to pituitary hypofunction, and an uncertain natural history. It is difficult to radiologically differentiate lymphocytic hypophysitis from pituitary macroadenoma, therefore, the gold standard of diagnosis remains histological. It is rarely reported in the elderly (>70 years old), however, given its unpredictable clinical course it remains an important differential diagnosis in patients of this age group who present with features suggestive of pituitary dysfunction. (C) 2015 Elsevier Ltd. All rights reserved.
机译:我们报道了一名73岁的女性患有淋巴细胞性垂体炎的妇女,该妇女具有非典型的临床特征,在放射学分析中似乎是垂体中风。淋巴细胞性垂体炎是垂体功能障碍的罕见原因,被认为是自身免疫性疾病。它通常会影响年轻的围产期妇女,其临床特征与垂体功能低下有关,并且自然史不确定。放射学上难以区分垂体巨腺瘤和淋巴细胞性垂体炎,因此诊断的金标准仍是组织学。在老年人(> 70岁)中很少报道,但是,由于其不可预测的临床过程,它仍然是这一年龄组患者的重要鉴别诊断,这些患者表现出垂体功能障碍。 (C)2015 Elsevier Ltd.保留所有权利。

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