Stan Marius N, Haglind Elizabeth G, Drake Matthew T
1 Department of Endocrinology, Mayo Clinic College of Medicine , Rochester, Minnesota.
2 Endocrinology Clinic of Minneapolis , Edina, Minnesota.
Thyroid. 2015 Sep;25(9):1055-9. doi: 10.1089/thy.2015.0212. Epub 2015 Aug 17.
Riedel's thyroiditis (RT) is a rare, fibroinflammatory condition which induces gradual thyroid gland destruction and adjacent soft-tissue fibrous infiltration. About one- seventh of RT cases are associated with hypoparathyroidism, necessitating long-term therapy for symptomatic hypocalcemia. The reversibility of the parathyroid hormone deficit has not been fully described.
A 40-year-old woman with no prior history of thyroid disease presented with a six month history of progressive thyroid enlargement complicated by worsening dysphagia and positional dyspnea. Her past medical history was remarkable only for retroperitoneal fibrosis. Physical examination revealed a large, hard, non-mobile goiter. Thyroid indices while maintained on levothyroxine were normal, but marked asymptomatic hypocalcemia with an inappropriately normal parathyroid hormone level was noted. Thyroid imaging and fine needle aspiration were consistent with RT. Isthmectomy and subsequent serial corticosteroid and tamoxifen treatment led to rapid symptom improvement. Serum calcium and parathyroid hormone levels returned to the reference range within three months.
We describe a case of RT in which hypoparathyroidism resolved after treatment targeted the mechanical compression and the fibroinflammatory milieu of the patient's thyroidal disease.
RT can be associated with hypoparathyroidism that is clinically silent at presentation. Mechanical decompression of the goiter and immunomodulatory therapy can reverse the fibrosclerotic process and lead to rapid recovery of parathyroid gland function, as in this patient. However, in most cases hypoparathyroidism is persistent and requires continued treatment to prevent symptomatic hypocalcemia.
里德尔甲状腺炎(RT)是一种罕见的纤维炎症性疾病,可导致甲状腺逐渐破坏及相邻软组织纤维浸润。约七分之一的RT病例与甲状旁腺功能减退有关,需要对有症状的低钙血症进行长期治疗。甲状旁腺激素缺乏的可逆性尚未得到充分描述。
一名40岁女性,既往无甲状腺疾病史,出现进行性甲状腺肿大6个月,伴有吞咽困难加重和体位性呼吸困难。她的既往病史仅因腹膜后纤维化而显著。体格检查发现一个大的、坚硬的、不可移动的甲状腺肿。服用左甲状腺素期间甲状腺指标正常,但发现有明显的无症状性低钙血症,甲状旁腺激素水平正常但不恰当。甲状腺成像和细针穿刺与RT一致。峡部切除术及随后的系列皮质类固醇和他莫昔芬治疗使症状迅速改善。血清钙和甲状旁腺激素水平在三个月内恢复到参考范围。
我们描述了一例RT病例,其中甲状旁腺功能减退在针对患者甲状腺疾病的机械压迫和纤维炎症环境进行治疗后得到缓解。
RT可伴有甲状旁腺功能减退,在发病时临床上无症状。如该患者所示,甲状腺肿的机械减压和免疫调节治疗可逆转纤维硬化过程并导致甲状旁腺功能迅速恢复。然而,在大多数情况下,甲状旁腺功能减退是持续性的,需要持续治疗以预防有症状的低钙血症。