S3478 A Case of Hypercalcemia Induced Acute Pancreatitis

Introduction: Acute pancreatitis is a common abdominal concern; however, hypercalcemia is a rare etiology. Hypercalcemia induced pancreatitis has been previously reported in individuals with multiple myeloma or multiple parathyroid adenomas. We present a case of acute pancreatitis induced by hypercalcemia in a patient with a single parathyroid adenoma. Case Description/Methods: A 55-year-old woman with no significant past medical history presents with acute epigastric pain with associated nausea and vomiting. Initial lab work revealed elevated calcium of 12.4 mg/dL, elevated lipase of 1,121 Units/L, intact parathyroid hormone (PTH) elevated at 165 pg/mL, and vitamin D levels were low at 11 ng/mL. Computed tomography scan revealed acute pancreatitis and 2.6 cm nodule that extended inferiorly off of the left thyroid lobe. Right upper quadrant ultrasound revealed cholelithiasis and gallbladder wall thickening, concerning for possible gallstone pancreatitis. However, magnetic resonance cholangiopancreatography (MRCP) revealed no evidence for choledocholithiasis and no biliary or pancreatic duct dilatation. Cholecystectomy was performed. Her symptoms continued to flare despite cholecystectomy. Endocrinology was consulted for hypercalcemia. Radionuclide parathyroid scintigraphy revealed left inferior gland uptake, consistent with parathyroid adenoma. Twenty-four-hour urine calcium and creatinine ruled out familial hypocalciuric hypercalcemia. Due to these findings, she then underwent left inferior parathyroidectomy with an appropriate drop of the intraoperative PTH from 325 pg/mL to 61 pg/mL. Pathology revealed atypical parathyroid adenoma. She was supplemented with 50,000 international units of vitamin D and 1 g elemental calcium to decrease the risk of post-op hypocalcemia. Discussion: Hypercalcemia induced pancreatitis due to parathyroid adenoma is a curable cause of pancreatitis and is an indication for adenoma resection, especially in symptomatic cases. This diagnosis is often disregarded in setting of more common etiologies like in our patient's case, which led to an unnecessary inpatient cholecystectomy, excessive use of hospital resources, and longer hospital stay. Our case highlights the importance of multispecialty care in early diagnosis and broader investigation of etiology of pancreatitis, as delay may lead to worsening pancreatitis.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001141372.38048.93
Primary Topic
Bone and Joint Diseases
Type
article
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0.00
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article

S3478 A Case of Hypercalcemia Induced Acute Pancreatitis

William Lai, Hyder Alikhan, Chelsea Edirisuriya, Sharan Parikh et al.
The American Journal of Gastroenterology
Bone and Joint Diseases
article

S3478 A Case of Hypercalcemia Induced Acute Pancreatitis

William Lai, Hyder Alikhan, Chelsea Edirisuriya, Sharan Parikh, Kunal Dalal
article en

Abstract

Introduction: Acute pancreatitis is a common abdominal concern; however, hypercalcemia is a rare etiology. Hypercalcemia induced pancreatitis has been previously reported in individuals with multiple myeloma or multiple parathyroid adenomas. We present a case of acute pancreatitis induced by hypercalcemia in a patient with a single parathyroid adenoma. Case Description/Methods: A 55-year-old woman with no significant past medical history presents with acute epigastric pain with associated nausea and vomiting. Initial lab work revealed elevated calcium of 12.4 mg/dL, elevated lipase of 1,121 Units/L, intact parathyroid hormone (PTH) elevated at 165 pg/mL, and vitamin D levels were low at 11 ng/mL. Computed tomography scan revealed acute pancreatitis and 2.6 cm nodule that extended inferiorly off of the left thyroid lobe. Right upper quadrant ultrasound revealed cholelithiasis and gallbladder wall thickening, concerning for possible gallstone pancreatitis. However, magnetic resonance cholangiopancreatography (MRCP) revealed no evidence for choledocholithiasis and no biliary or pancreatic duct dilatation. Cholecystectomy was performed. Her symptoms continued to flare despite cholecystectomy. Endocrinology was consulted for hypercalcemia. Radionuclide parathyroid scintigraphy revealed left inferior gland uptake, consistent with parathyroid adenoma. Twenty-four-hour urine calcium and creatinine ruled out familial hypocalciuric hypercalcemia. Due to these findings, she then underwent left inferior parathyroidectomy with an appropriate drop of the intraoperative PTH from 325 pg/mL to 61 pg/mL. Pathology revealed atypical parathyroid adenoma. She was supplemented with 50,000 international units of vitamin D and 1 g elemental calcium to decrease the risk of post-op hypocalcemia. Discussion: Hypercalcemia induced pancreatitis due to parathyroid adenoma is a curable cause of pancreatitis and is an indication for adenoma resection, especially in symptomatic cases. This diagnosis is often disregarded in setting of more common etiologies like in our patient's case, which led to an unnecessary inpatient cholecystectomy, excessive use of hospital resources, and longer hospital stay. Our case highlights the importance of multispecialty care in early diagnosis and broader investigation of etiology of pancreatitis, as delay may lead to worsening pancreatitis.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 60%
Bone and Joint Diseases
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