首页> 外文期刊>European journal of endocrinology >Glucocorticoid-responsive lymphocytic parathyroiditis and hypocalciuric hypercalcemia due to autoantibodies against the calcium-sensing receptor: a case report and literature review
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Glucocorticoid-responsive lymphocytic parathyroiditis and hypocalciuric hypercalcemia due to autoantibodies against the calcium-sensing receptor: a case report and literature review

机译:针对钙敏感受体的自身抗体引起的糖皮质激素反应性淋巴细胞性甲状旁腺炎和低钙血症性高钙血症:一例病例并文献复习

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Objective Autoimmune lymphocytic parathyroiditis and acquired hypocalciuric hypercalcemia associated with autoantibodies against the calcium-sensing receptor (anti-CaSR) are rare and poorly understood conditions. Here, we describe a patient with acquired parathyroid hormone (PTH)-dependent hypercalcemia with associated hypocalciuria, found to have true lymphocytic parathyroiditis on histopathology, and circulating anti-CaSR antibodies in serum. Design and methods A 64-year-old woman was referred to our clinic for persistent hypercalcemia after a subtotal parathyroidectomy. She was normocalcemic until the age of 63 years when she was diagnosed with primary hyperparathyroidism. She underwent subtotal parathyroidectomy with appropriate intraoperative PTH decline. Two weeks post-parathyroidectomy, she presented with persistent hypercalcemia and hyperparathyroidism. Urine studies revealed an inappropriately low 24-h urine calcium (Ca)/creatinine clearance ratio. Surgical pathology was consistent with true lymphocytic parathyroiditis with lymphoid follicles. The presence of circulating anti-CaSR antibodies was detected by immunoprecipitation of CaSR by the patient’s serum. After a 4-week course of prednisone, serum Ca and PTH normalized, and her anti-CaSR titers declined. She remains normocalcemic 10 months after the discontinuation of glucocorticoid therapy. We present this patient in the context of the relevant published literature on lymphocytic parathyroiditis and acquired hypocalciuric hypercalcemia related to anti-CaSR antibodies. Conclusions Autoimmune lymphocytic parathyroiditis and acquired hypocalciuric hypercalcemia associated with anti-CaSR antibodies is a very rare yet important condition to be considered in a patient with acquired PTH-dependent hypercalcemia with inappropriate hypocalciuria. Although subtotal parathyroidectomy is unlikely to correct the hypercalcemia, this entity may respond to a short course of prednisone therapy.
机译:目的自身免疫性淋巴细胞性甲状旁腺炎和获得性低钙血症性高钙血症与针对钙敏感受体(anti-CaSR)的自身抗体相关,是罕见的且了解甚少的疾病。在这里,我们描述了一名患有获得性甲状旁腺激素(PTH)依赖性高钙血症并伴有低钙尿症的患者,该患者在组织病理学上具有真正的淋巴细胞性甲状旁腺炎,并且血清中存在循环的抗CaSR抗体。设计与方法甲状旁腺全切除术后,一名64岁妇女因持续高钙血症而被转诊至我们的诊所。直到63岁被诊断出患有原发性甲状旁腺功能亢进时,她才保持正常血钙状态。她接受了大部的甲状旁腺切除术,术中PTH适当降低。甲状旁腺切除术后两周,她表现出持续的高钙血症和甲状旁腺功能亢进。尿液研究显示24小时尿钙(Ca)/肌酐清除率过低。手术病理与真正的淋巴细胞性甲状旁腺炎伴淋巴滤泡一致。通过患者血清对CaSR的免疫沉淀来检测循环中抗CaSR抗体的存在。泼尼松4周疗程后,血清Ca和PTH恢复正常,她的抗CaSR滴度下降。糖皮质激素治疗终止后10个月,她仍保持正常血钙状态。我们在有关淋巴细胞性甲状旁腺炎和与抗CaSR抗体相关的获得性低钙血症性高钙血症的相关已发表文献的背景下介绍了该患者。结论自身免疫性淋巴细胞性甲状旁腺炎和获得性低钙血症与抗CaSR抗体相关,对于患有获得性PTH依赖性高钙血症并伴有低钙血症的患者,是一种非常罕见但重要的疾病。尽管进行亚全区甲状旁腺切除术不可能纠正高钙血症,但该实体可能对泼尼松治疗的短期疗程有反应。

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