Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2016) 41 EP182 | DOI: 10.1530/endoabs.41.EP182

ECE2016 Eposter Presentations Calcium and Vitamin D metabolism (61 abstracts)

Clinical case of chronic calcific pancreatitis in a patient with parathyroid carcinoma caused primary hyperparathyroidism

Timur Britvin , Vyacheslav Ignatyuk & Armine Kazarian


State Budget Institution of Health of the Moscow region “Moscow Regional Research Clinical Institute”, Moscow, Russia.

Parathyroid carcinoma is a rare cause of primary hyperparathyroidism (PHPT) and is usually presented with severe hypercalcaemia and parathyroid hormone (PTH) elevation. Hypercalcaemia can lead to calcification of parenchymatous organs, including pancreas, and acute or chronic pancreatitis.

Case report: A 46-year-old woman was admitted to the endocrine surgery department of our institution with severe weakness, appetite and weight loss (25 kg in a year), abdominal and joint pain, apathy, skin dryness. Laboratory tests: PTH 2517.4 pg/ml (11–62), total serum calcium 3.36 mmol/l (2.2–2.6), ionized serum calcium 2.14 mmol/l (1.12–1.32), amylase 1280 U/l (<100). Neck US: left lobe of thyroid gland is presented with a heterogenous nodule with cystic degeneration, 5.0×3.0×3.5 cm. Neck CT-scan: a 37×26×51 mm mass near the back margin of left thyroid lobe, 53 HU density in the native examination, 64 HU in the arterial phase of contrast examination and 50 HU in the venous phase. The upper pole of the tumor is located at the thyroid cartilage, the lower pole of the tumor is in the mediastinum. Abdomen CT-scan: pancreas is located normally, with uneven margins and multiple calcifications. A 12 mm cyst in the body of pancreas and a cyst of irregular shape in the tail with thick calcificated border (78×46×48 mm) are detected. Pancreatic duct is not dilated.

At first, parathyroid tumor resection and hemithyroidectomy were performed. After the surgery PTH lowered to 193 pg/ml and hypocalcaemia (total Ca 1.91 mmol/l, ionized Ca 0.94 mmol/l) occurred, treated with calcium and vitamin D supplement. Parathyroid carcinoma was confirmed by histology. Two months later subtotal distal pancreatectomy and splenectomy were performed. Three months after the treatment the patient’s health improved, abdominal pain disappeared and she gained 5 kg. PHPT is not persisting.

This case report shows that chronic calcific cystic pancreatitis can develop on the background of hypercalcaemia and improve after parathyroid tumor resection. We suggest that serum calcium and PTH should be measured in all patients with non-alcoholic and non-biliary pancreatitis for PHPT diagnostic and pancreatitis should be diagnosed in all patients with PHPT.

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