肢端肥大症性心肌病患者在过度生长激素分泌得到控制后双心室肥厚的消退
Regression of biventricular hypertrophy in acromegalic cardiomyopathy following management of excessive growth hormone secretion.
作者信息
Faraj Raid, Diallo Thierno Hamidou, Abdelali Mehdi, Lahjouji Reda, Benmessaoud Fatima-Azzahra, Doghmi Nawal, Zarzur Jamila, Cherti Mohamed
机构信息
Cardiology B Department, Ibn Sina University Hospital, Mohammed V University of Rabat, Angle avenue Allal El Fassi et Mfadel Cherkaoui, Al Irfane - 8007, N.U, Morocco.
出版信息
Oxf Med Case Reports. 2024 Oct 10;2024(10):omae112. doi: 10.1093/omcr/omae112. eCollection 2024 Oct.
Acromegalic cardiomyopathy is a significant cardiovascular complication associated with acromegaly, caused by excessive growth hormone production from a pituitary adenoma. Early diagnosis can be challenging due to its insidious nature. This case underscores the critical significance of timely medical intervention, illustrating favorable outcomes resulting from prompt therapeutic measures.
肢端肥大症性心肌病是一种与肢端肥大症相关的严重心血管并发症，由垂体腺瘤分泌过多生长激素引起。由于其隐匿性，早期诊断可能具有挑战性。本病例强调了及时医疗干预的关键意义，说明了及时采取治疗措施所带来的良好结果。
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