Undiagnosed acromegaly as an underlying cause of sudden death.
Anna Elisabet BorgenAnne Birgitte Dyhre BuggeEva Løbner LundJytte BannerPublished in: Forensic science, medicine, and pathology (2021)
We report a case of sudden death in a 31-year-old male diagnosed at autopsy with clinical undiagnosed acromegaly. The purpose of this report is to underline the importance of health professionals reacting to phenotypic acromegaly, such as acral enlargement and/or unexplained hypertension, including a range of severe comorbidities, to avoid a fatal outcome. Recent studies have shown that the increased mortality seen in acromegaly patients can be reversed with modern treatment aimed at normalizing GH and IGF-I levels. One year before death, the presented case was diagnosed with hypertension, but was otherwise described as healthy. The forensic autopsy, including post-mortem CT, showed phenotypic facial and body characteristics for acromegaly, general visceromegaly, and a pituitary tumor. The cause of death was heart failure due to end-stage acromegalic cardiopathy. Because the disease is slowly progressive, the individual himself, and the people close to him, might not have considered the acromegaly-related facial changes as abnormal.
Keyphrases
- growth hormone
- heart failure
- blood pressure
- end stage renal disease
- newly diagnosed
- ejection fraction
- multiple sclerosis
- chronic kidney disease
- early onset
- magnetic resonance imaging
- prognostic factors
- magnetic resonance
- left ventricular
- cardiovascular disease
- positron emission tomography
- binding protein
- cell proliferation
- pi k akt
- dual energy