PMID- 33936819 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20210504 IS - 2090-6501 (Print) IS - 2090-651X (Electronic) IS - 2090-651X (Linking) VI - 2021 DP - 2021 TI - "Primary Hyperparathyroidism (PHPT) in Children: Two Case Reports and Review of the Literature". PG - 5539349 LID - 10.1155/2021/5539349 [doi] LID - 5539349 AB - Primary hyperparathyroidism (PHPT) is a rare disorder in children and adolescents. Typical biochemical features are hypercalcemia and hypophosphatemia, but the clinical features can be heterogeneous, and in some cases, symptoms are vague and nonspecific, leading to misdiagnosis or late diagnosis. Herein, we report two cases of PHPT in pediatric age with different presenting symptoms, pain in the foot, and progressive alteration of the gait in the first case and recurrent abdominal pain with emotional lability in the second. Biochemical and radiological assessment confirmed PHPT. Both cases were treated surgically as definitive treatment, but in the second case, previous medical treatment with cinacalcet, a calcimimetic agent, was required to reduce serum PTH and calcium levels. After surgery, despite conventional treatment with calcium and calcitriol, case 1 developed a hungry bone syndrome. The analysis of the MEN-1 (Multiple Endocrine Neoplasia) gene was negative in both cases. A diagnosis of PHPT should be considered when children or adolescents present bone pain with radiological imaging of osteolytic lesion and biochemical feature of hypercalcemia associated with hypophosphatemia. In PHPT, the gold standard treatment is represented by surgery followed by strict postoperative endocrine monitoring to maintain adequate homeostasis of calcium and bone metabolism. CI - Copyright (c) 2021 Gerdi Tuli et al. FAU - Tuli, Gerdi AU - Tuli G AUID- ORCID: 0000-0001-5862-8958 AD - Department of Pediatric Endocrinology, Regina Margherita Children's Hospital of Turin, Turin, Italy. AD - Department of Sciences of Public Health and Pediatrics, University of Turin, Turin, Italy. FAU - Munarin, Jessica AU - Munarin J AUID- ORCID: 0000-0002-5075-8448 AD - Department of Pediatric Endocrinology, Regina Margherita Children's Hospital of Turin, Turin, Italy. AD - Department of Sciences of Public Health and Pediatrics, University of Turin, Turin, Italy. FAU - Tessaris, Daniele AU - Tessaris D AUID- ORCID: 0000-0002-6484-4371 AD - Department of Pediatric Endocrinology, Regina Margherita Children's Hospital of Turin, Turin, Italy. AD - Department of Sciences of Public Health and Pediatrics, University of Turin, Turin, Italy. FAU - Buganza, Raffaele AU - Buganza R AUID- ORCID: 0000-0003-1850-2300 AD - Department of Pediatric Endocrinology, Regina Margherita Children's Hospital of Turin, Turin, Italy. AD - Department of Sciences of Public Health and Pediatrics, University of Turin, Turin, Italy. FAU - Matarazzo, Patrizia AU - Matarazzo P AUID- ORCID: 0000-0001-7601-786X AD - Department of Pediatric Endocrinology, Regina Margherita Children's Hospital of Turin, Turin, Italy. AD - Department of Sciences of Public Health and Pediatrics, University of Turin, Turin, Italy. FAU - De Sanctis, Luisa AU - De Sanctis L AUID- ORCID: 0000-0003-2113-6196 AD - Department of Pediatric Endocrinology, Regina Margherita Children's Hospital of Turin, Turin, Italy. AD - Department of Sciences of Public Health and Pediatrics, University of Turin, Turin, Italy. LA - eng PT - Case Reports DEP - 20210413 PL - United States TA - Case Rep Endocrinol JT - Case reports in endocrinology JID - 101576457 PMC - PMC8060104 COIS- All authors declare no conflicts of interest. EDAT- 2021/05/04 06:00 MHDA- 2021/05/04 06:01 PMCR- 2021/04/13 CRDT- 2021/05/03 06:18 PHST- 2021/02/02 00:00 [received] PHST- 2021/03/29 00:00 [revised] PHST- 2021/04/08 00:00 [accepted] PHST- 2021/05/03 06:18 [entrez] PHST- 2021/05/04 06:00 [pubmed] PHST- 2021/05/04 06:01 [medline] PHST- 2021/04/13 00:00 [pmc-release] AID - 10.1155/2021/5539349 [doi] PST - epublish SO - Case Rep Endocrinol. 2021 Apr 13;2021:5539349. doi: 10.1155/2021/5539349. eCollection 2021.