Babar Ghufran, Alemzadeh Ramin
Section of Pediatric Endocrinology, Children's Mercy Hospitals and Clinics, 3101 Broadway Boulevard, Kansas City, MO 64111, USA.
Division of Pediatric Endocrinology, University of Illinois College of Medicine at Chicago, 1853 W. Polk Street, Chicago, IL 60612, USA.
Case Rep Endocrinol. 2014;2014:937631. doi: 10.1155/2014/937631. Epub 2014 Mar 30.
Primary hyperparathyroidism (PHPT) is a disorder of calcium homeostasis. We report the case of a 17-year-old adolescent male, who presented with an acute psychosis coinciding with severe hypercalcemia and markedly elevated intact parathyroid hormone (iPTH) level and low vitamin D level. A Sestamibi scan showed a positive signal inferior to the left lobe of the thyroid gland. He had only a partial response to the initial medical and psychiatric management. The enlarged parathyroid gland was resected surgically and postoperatively serum calcium and iPTH levels normalized. The histopathology was compatible with a benign adenoma. Patient's acute psychotic symptoms resolved gradually after surgery; however he remained under psychiatric care for the behavioral issues for about 6 months after surgery. While psychosis is a rare clinical manifestation of hypercalcemia secondary to PHPT in pediatric population, it should be considered as a clinical clue in an otherwise asymptomatic pediatric patient.
原发性甲状旁腺功能亢进症(PHPT)是一种钙稳态紊乱疾病。我们报告了一例17岁青少年男性病例,该患者出现急性精神病症状,同时伴有严重高钙血症、显著升高的甲状旁腺激素(iPTH)水平和低维生素D水平。锝-99m甲氧基异丁基异腈(Sestamibi)扫描显示甲状腺左叶下方有阳性信号。他对初始的药物和精神治疗仅部分有效。肿大的甲状旁腺被手术切除,术后血清钙和iPTH水平恢复正常。组织病理学结果与良性腺瘤相符。患者术后急性精神病症状逐渐缓解;然而,术后他因行为问题仍接受了约6个月的精神科治疗。虽然精神病是儿童人群中PHPT继发高钙血症的罕见临床表现,但在无症状的儿科患者中应将其视为临床线索。