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- W3029423983 abstract "Four cases of pituitary acromegalic cardiomyopathy were reported and relative literature was reviewed in this article. Four patients were all males aged 45-63 y. The patients were diagnosed as pituitary adenoma, then NYHA grade Ⅲ-Ⅳ heart failure developed. One patient had both acromegaly and coronary heart disease, and all patients had arrhythmia attacks. The growth hormone levels were not under control in 3 patients, and for the remaining patient with normalized growth hormone the end-stage heart failure also developed. The onset of pituitary acromegalic cardiomyopathy is hidden; when the disease progresses to advanced heart failure, the prognosis would be poor in most cases. So early diagnosis and timely treatment is of great importance in acromegalic cardiomyopathy.Key words: Acromegaly; Cardiomyopathies" @default.
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- W3029423983 date "2014-10-04" @default.
- W3029423983 modified "2023-09-23" @default.
- W3029423983 title "Pituitary acromegalic cardiomyopathy: a report of 4 cases and literature review" @default.
- W3029423983 doi "https://doi.org/10.3760/cma.j.issn.1671-7368.2014.10.016" @default.
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