Aortic root dilation in acromegaly.
Yvette Ayewa Yeboah-KordiehWaqar ArifDavid S WeismanRoberto SalvatoriPublished in: BMJ case reports (2024)
Previous studies have linked persistent elevations in growth hormone (GH) and insulin-like growth factor-1 (IGF-1) to cardiac abnormalities including aortic root dilation. Guidelines in the management of this dilation below the size recommended for surgery have not been well defined but follow-up and intervention when appropriate could be life-saving. We report the case of a man in his 60s who had been living with undiagnosed acromegaly for many years. His initial assessment through point-of-care ultrasound raised concerns about potential cardiac enlargement, prompting further investigation with a formal echocardiogram, which revealed a significant aortic root dilation measuring 4.5 cm. Subsequent blood tests confirmed elevated levels of IGF-1. Brain MRI showed a focal lesion in the pituitary gland, which was surgically resected, confirming the diagnosis of a GH-secreting pituitary adenoma. One year after surgery, a repeat CT angiogram of the chest demonstrated a stable size of the aortic root aneurysm.
Keyphrases
- growth hormone
- left ventricular
- aortic valve
- pulmonary artery
- aortic dissection
- contrast enhanced
- magnetic resonance imaging
- minimally invasive
- computed tomography
- randomized controlled trial
- heart failure
- resting state
- magnetic resonance
- functional connectivity
- pulmonary arterial hypertension
- risk assessment
- dual energy
- atrial fibrillation
- abdominal aortic aneurysm
- clinical evaluation
- surgical site infection
- contrast enhanced ultrasound