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首页> 外文期刊>Journal of the Saudi Heart Association >Sheehan’s syndrome with reversible dilated cardiomyopathy: A case report and brief overview
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Sheehan’s syndrome with reversible dilated cardiomyopathy: A case report and brief overview

机译:希恩氏综合征伴可逆性扩张型心肌病:一例病例报告和简要概述

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摘要

Sheehan’s syndrome is a rare condition characterized by post-partal panhypopituitarism due to necrosis of adenohypophysis resulting from severe post-partum hemorrhage. Lethargy, amenorrhea and failure of lactation are the usual presenting features. Cardiac involvement in Sheehan’s syndrome is rare. The case presented here describes dilated cardiomyopathy in a 36-year-old lady who failed to respond adequately to the standard anti-failure treatment. Further investigation revealed the diagnosis of Sheehan’s syndrome. Besides other manifestations, cardiac function reverted to normal after giving replacement therapy with glucocorticoid, levothyroxine and sex hormone. Physicians, specially those in developing countries, should have high index of suspicion for the diagnosis of Sheehan’s syndrome while dealing with a case of ‘peripartal dilated cardiomyopathy’. Persistent amenorrhea and failure of lactation may be important clues in this context. Timely diagnosis and appropriate treatment can lessen the sufferings of the patients.
机译:Sheehan综合征是一种罕见的疾病,其特征是严重的产后出血导致腺垂体坏死,导致部分性全垂体功能减退。嗜睡,闭经和泌乳失败是通常的表现。心脏参与希恩综合征的情况很少见。此处介绍的病例描述了一位36岁的女士的扩张型心肌病,该女士对标准的抗失败治疗没有足够的反应。进一步调查显示,希恩氏综合症的诊断。除其他表现外,给予糖皮质激素,左甲状腺素和性激素替代治疗后,心功能恢复正常。在处理“围产期扩张型心肌病”的同时,医师,尤其是发展中国家的医师,应具有较高的怀疑度,以诊断希恩氏综合症。在这种情况下,持续性闭经和泌乳失败可能是重要的线索。及时诊断和适当治疗可以减轻患者的痛苦。

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