Department of Neuroendocrinology and Bone Diseases, Endocrinology Research Centre, Moscow, Russian Federation.
Department and Laboratory of Inherited Endocrine Disorders, Endocrinology Research Centre, Moscow, Russian Federation.
Horm Res Paediatr. 2020;93(4):272-278. doi: 10.1159/000510625. Epub 2020 Sep 30.
Primary hyperparathyroidism (PHPT) is rare and usually symptomatic in children. There is no approved medication to lower serum calcium levels in this patient group. Denosumab is used in adult patients with osteoporosis and hyperparathyroidism. To our knowledge, only 1 case of denosumab treatment in a child with severe PHPT has been reported to date.
A 16-year-old female was referred to our clinic with symptoms including pathologic fractures, nausea, emesis, and progressive weight loss. At admission, her serum total calcium was 4.17 mmol/L (reference range 2.15-2.55), parathyroid hormone 2,151 pg/mL (15-65), and phosphate 1.07 mmol/L (1.45-1.78). Due to potentially life-threatening hypercalcemia, denosumab 60 mg subcutaneously was administered after obtaining informed consent. Serum calcium levels were reduced within 12 h of injection and the patient's condition rapidly improved, which allowed genetic testing to be done prior to surgery. A heterozygous mutation in the CDC73 gene was revealed, and a parathyroidectomy was performed on day 22 after denosumab administration. Morphological examination revealed solitary parathyroid adenoma. After surgery, hypocalcemia developed requiring high doses of alfacalcidol and calcium supplements.
Our case supports the previous observations in adults that denosumab can be safely and effectively used as a preoperative treatment in patients with PHPT and severe hypercalcemia and shows that it may be used in pediatric patients.
原发性甲状旁腺功能亢进症(PHPT)在儿童中罕见且通常有症状。在该患者群体中,没有批准的药物可以降低血清钙水平。地舒单抗用于治疗患有骨质疏松症和甲状旁腺功能亢进症的成年患者。据我们所知,迄今为止,仅报告了 1 例地舒单抗治疗严重 PHPT 儿童的病例。
一名 16 岁女性因包括病理性骨折、恶心、呕吐和进行性体重减轻在内的症状被转至我院就诊。入院时,其血清总钙为 4.17mmol/L(参考范围 2.15-2.55),甲状旁腺激素 2151pg/mL(15-65),磷酸盐 1.07mmol/L(1.45-1.78)。由于存在潜在危及生命的高钙血症,在获得知情同意后,给予地舒单抗 60mg 皮下注射。注射后 12 小时内血清钙水平降低,患者病情迅速改善,这使得可以在手术前进行基因检测。发现 CDC73 基因突变,在给予地舒单抗 22 天后进行甲状旁腺切除术。形态学检查显示为甲状旁腺腺瘤。手术后出现低钙血症,需要大剂量的骨化三醇和钙补充剂。
我们的病例支持先前在成年患者中观察到的地舒单抗可安全有效地用于 PHPT 和严重高钙血症患者的术前治疗,并表明其可用于儿科患者。