Abstract
To report an uncommon case of diabetic ketoacidosis in a patient with acromegaly, and present the clinical response to treatment. Patient evaluation and literature review. A 23-year-old Japanese male with no prior medical history, presented with diabetic ketoacidosis (DKA) and found to have acromegaly. His growth hormone (GH) level was 115 ng/ml, serum insulin-like growth factor-1 (IGF-1) was 1118 ng/ml, and cranial MRI showed a non-enhancing 2.4 x 1.7 x 2.0 cm pituitary mass. After transphenoidal hypophysectomy, his GH level decreased but his IGF-1 level remained unchanged, yet he required no anti-hyperglycemic medications and attained near normal A1c level of 5.8%. He subsequently underwent stereotactic radiotherapy, and additional treatment with bromocriptine and octreotide acetate were not effective, but pegvisomant therapy lowered his IGF-1 concentration to targeted levels. The cause of DKA in this patient with acromegaly is most likely due to glucotoxicity and lipotoxicity, which cause severe but partially reversible β-cell dysfunction; possibly categorized within the syndromes of Ketosis-Prone Diabetes Mellitus (KPD). Diabetic ketoacidosis is an uncommon initial presentation of acromegaly. Successful reduction of GH excess appears to control and resolve hyperglycemia.
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More From: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
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