Abstract
BackgroundPatients with growth hormone (GH)-secreting adenoma usually develop glucose intolerance. GH increases metabolic rate and, when secreted aberrantly, may result in metabolic syndrome. Herein, we examine the associations of pituitary tumor-induced secretion of hormone with insulin resistance and metabolic syndrome, and determine the relation of pituitary tumor apoplexy-induced diabetic ketoacidosis (DKA) and acute pancreatitis.Case presentationA 44-year-old male with a history of hypertension presented to the emergency department of our hospital on February 14, 2019 with symptoms of headache, dizziness, and vomiting. Computed tomography of the head revealed pituitary tumor with bleeding. An ultrasound scan of the abdomen revealed fatty liver and acute pancreatitis. Further examination revealed the presence of DKA, hypertriglyceridemia, cortical hypofunction crisis and acute kidney injury. Surgical endoscopic resection of the pituitary tumor resection via the transsphenoidal approach was performed. The patient’s postoperative recovery was remarkable.ConclusionsLong-term growth hormone abnormality may trigger insulin resistance, leading to metabolic syndrome and impaired glucose and lipid metabolism. The pituitary adenoma apoplexy may also directly induce DKA, creating a domino effect, which further deteriorate the aberrant metabolism of glucose and lipids.
Highlights
Patients with growth hormone (GH)-secreting adenoma usually develop glucose intolerance
The pituitary adenoma apoplexy may directly induce diabetic ketoacidosis (DKA), creating a domino effect, which further deteriorate the aberrant metabolism of glucose and lipids
Coexistence of impaired glucose metabolism, hyperinsulinemia, hypertriglyceridemia (HTG), and hypertension is characteristic of metabolic syndrome (MetS), a cluster of five individual risk factors, including hyperglycemia, hypertriglyceridemia, hypertension, abnormal lipid metabolism and abdominal obesity [2]
Summary
Long-term growth hormone abnormality may trigger insulin resistance, leading to metabolic syndrome and impaired glucose and lipid metabolism.
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