Parathyroid Apoplexy Following Cinacalcet Treatment in Primary Hyperparathyroidism

被引:3
作者
Di Dalmazi, Giulia
Giuliani, Cesidio [1 ]
Napolitano, Giorgio
机构
[1] Univ G dAnnunzio, Unit Endocrinol, Dept Med & Sci Aging, Chieti, Italy
关键词
parathyroid apoplexy; cinacalcet; primary hyperparathyroidism; hungry bone syndrome; hypocalcemia; SERUM-CALCIUM; DOUBLE-BLIND; HYPERPLASIA; REMISSION;
D O I
10.3389/fendo.2018.00777
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cinacalcet, a calcimimetic drug, is considered a safe and valid option for the treatment of hypercalcemia in patients with primary hyperparathyroidism who are unable to undergo parathyroidectomy. Hypocalcemia and gastrointestinal adverse reactions are the main side effects reported in patients treated with cinacalcet. We present here the case of an 80-years-old patient with primary hyperparathyroidism treated with cinacalcet for 17 months who developed a severe and symptomatic episode of hypocalcemia requiring hospitalization 1 month after reaching a daily dose of 180 mg. Follow-up laboratory and imaging exams showed remission of primary hyperparathyroidism and disappearance of the parathyroid adenoma, suggesting a possible association between cinacalcet therapy and parathyroid infarction resulting in normalization of the elevated serum parathyroid hormone levels and severe hypocalcemia. No known cases of iatrogenic parathyroid apoplexy have thus far been described. We report here the first case of parathyroid apoplexy associated with the administration of cinacalcet in a patient with primary hyperparathyroidism. Parathyroid apoplexy features heterogeneous clinical manifestations ranging from relatively asymptomatic to potentially life-threatening cases. The occurrence of this complication should be carefully considered in patients with primary hyperparathyroidism in therapy with cinacalcet.
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