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Postoperative hungry bone syndrome in primary hyperparathyroidism: A case report
Bin Li1, XiaoXu Lv, XiaoMing Li
1Department of Otorhinolaryngology, Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Hungry bone syndrome (HBS) is a rare cause of severe hypocalcemia after parathyroidectomy (PTX). This case highlights HBS management and predictors to reduce its incidence and duration.
Area of Science:
- Endocrinology
- Surgical Oncology
- Nephrology
Background:
- Hungry bone syndrome (HBS) is an underdiagnosed cause of severe hypocalcemia post-parathyroidectomy (PTX).
- It occurs in patients with high bone turnover, where decreased parathyroid hormone leads to excessive calcium resorption.
- Associated hypophosphatemia and hypomagnesemia can occur.
Purpose of the Study:
- To present a case of HBS following PTX for a parathyroid adenoma.
- To summarize predictors and perioperative management strategies for HBS.
Main Methods:
- A 57-year-old woman with symptomatic hyperparathyroidism underwent PTX for a parathyroid adenoma.
- Postoperative HBS was diagnosed on day 3 and managed with calcium supplementation and other interventions.
- The patient's condition resolved over 9 days, with discharge on day 13.
Main Results:
- The patient experienced a 9-day episode of HBS post-PTX.
- Successful management with calcium supplementation and pharmacological interventions led to normalization of parameters.
- The patient was discharged on postoperative day 13.
Conclusions:
- HBS is a critical consideration in patients with primary hyperparathyroidism undergoing PTX.
- Identifying predictors and optimizing perioperative management can mitigate HBS severity and duration.
- This case underscores the importance of prompt diagnosis and treatment of HBS.
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