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[肢端肥大症性心肌病]

[Acromegalic myocardiopathy].

作者信息

Clemente Gallego David, Gómez Bueno Manuel, Lucas Morante Tomás

机构信息

Servicio de Endocrinología y Nutrición, Hospital Universitario Puerta de Hierro, Madrid, Spain.

出版信息

Endocrinol Nutr. 2009 Feb;56(2):96-8. doi: 10.1016/S1575-0922(09)70558-3. Epub 2009 May 1.

Abstract

Acromegaly is characterized by chronic growth hormone hypersecretion. Cardiovascular alterations such as hypertension, left ventricular hypertrophy, cardiac rhythm disturbances and valvular disease are common in this disease and are the main cause of death. Control of acromegaly by surgery or pharmacotherapy has been shown to improve cardiovascular morbidity. We report a case of acromegalic myocardiopathy in a 59-year-old woman with dilated myocardiopathy who presented ventricular diameter and contractility normalization following medical treatment.

摘要

肢端肥大症的特征是慢性生长激素分泌过多。心血管改变,如高血压、左心室肥厚、心律失常和瓣膜疾病在这种疾病中很常见,并且是主要死因。通过手术或药物治疗控制肢端肥大症已被证明可改善心血管疾病的发病率。我们报告一例59岁患有扩张型心肌病的肢端肥大症性心肌病女性病例,该患者在接受药物治疗后心室直径和收缩力恢复正常。

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