Acute pancreatitis. A rare complication of primary hyperparathyroidism (pHPT)

Citation
M. Kronberger et al., Acute pancreatitis. A rare complication of primary hyperparathyroidism (pHPT), MONATS KIND, 149(4), 2001, pp. 373-376
Citations number
30
Categorie Soggetti
Pediatrics
Journal title
MONATSSCHRIFT KINDERHEILKUNDE
ISSN journal
00269298 → ACNP
Volume
149
Issue
4
Year of publication
2001
Pages
373 - 376
Database
ISI
SICI code
0026-9298(200104)149:4<373:APARCO>2.0.ZU;2-G
Abstract
Background. Primary hyperparathyroidism (pHPT) in childhood and adolescence is a rare disease. Therefore diagnosis often is delayed. Methods. We report an a 13 year old boy, who sufferd from nausea,abdominal pain and weight loss for 9 months. We diagnosed an adenoma of the parathyro id gland and an acute pancreatitis in the course of a hypercalcemic crisis. Results. After stabilizing the patient, the adenoma was removed surgically. No problems occured after the surgical treatment. Within 3 months the boy regained his original weight. Conclusion. Symptoms like nausea, abdominal pain, cephalea, hypertonia, ano rexia and renal stones could be a hint for pHPT. The coincidence of pHPT an d pancreatitis is extremely rare. According to references in the literatur this association is most likely related to elevated calcium levels due to a dvanced pHPT.