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A 50-year-old man with severe hypercalcemia: a case report.
K Van den Hauwe1, S G Oeyen, B F Schrijvers
1Department of Emergency Medicine Ghent University Hospital, Belgium. kristof_van_den_hauwe@hotmail.com
Early diagnosis and treatment of acute severe hypercalcemic syndrome due to primary hyperparathyroidism are crucial. Prompt management of this rare endocrine emergency, often caused by parathyroid adenoma, can reduce mortality.
Area of Science:
- Endocrinology
- Nephrology
- Oncology
Background:
- Primary hyperparathyroidism can lead to acute severe hypercalcemic syndrome, a rare but life-threatening endocrine emergency.
- Undiagnosed parathyroid adenoma is a common cause of this condition, necessitating prompt recognition.
Observation:
- A 50-year-old male presented with non-specific symptoms including anorexia, nausea, vomiting, polyuria, dehydration, abdominal pain, weight loss, fatigue, muscular weakness, irritability, and lethargy.
- Markedly elevated serum calcium (23.6 mg/dL) and parathyroid hormone (PTH) (>1900 ng/L) levels confirmed severe hypercalcemia.
- Despite initial treatment, symptoms persisted, leading to transfer to an intensive care unit for stabilization.
Findings:
- A parathyroid adenoma was diagnosed as the cause of the hypercalcemia.
- Surgical intervention (parathyroidectomy) was performed, resulting in an uneventful postoperative recovery.
- The patient was discharged in good general condition following successful treatment.
Implications:
- This case highlights the critical importance of early diagnosis and management of acute primary hyperparathyroidism to prevent severe hypercalcemic syndrome.
- Prompt recognition and intervention are vital for reducing mortality associated with this endocrine emergency.
- While surgical treatment is definitive, mortality rates remain significant if the condition is not promptly addressed.
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