原发性甲状旁腺功能亢进症导致的头颅下垂对 evocalcet 的治疗反应良好:病例报告

IF 0.4 Q4 CLINICAL NEUROLOGY
Hiroyuki Sumikura, Hiromitsu Miyakawa, Takahiro Tomoda, Takuma Sato, Mai Ito, Yuki Shimada, Yoshiyasu Ueda, Manabu Sakaguchi
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引用次数: 0

摘要

一名83岁的妇女出现了急性垂头综合征(DHS),并伴有颈部局部肌无力。血清钙和完整甲状旁腺激素(iPTH)水平分别升高至 12.2 mg/dL 和 173 pg/mL,99m锝-MIBI 闪烁扫描显示甲状旁腺功能亢进。肌电图显示颈后伸肌具有肌病特征。原发性甲状旁腺功能亢进症(PHPT)相关肌病被诊断为DHS的病因。口服 evocalcet 可改善 DHS,并使升高的血清钙水平恢复正常,但 iPTH 水平仍然升高。随后,甲状旁腺切除术将 iPTH 水平降至正常,DHS 也不再复发。以DHS为首发症状的PHPT病例极为罕见,据我们所知,这是第一例用evocalcet缓解DHS的病例。因此,血清 iPTH 水平不一定与肌无力相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A good therapeutic response to evocalcet for dropped head due to primary hyperparathyroidism: A case report
An 83‐year‐old woman presented with an acute course of dropped head syndrome (DHS) with muscle weakness localized to the neck. Serum calcium and intact parathyroid hormone (iPTH) levels were elevated to 12.2 mg/dL and 173 pg/mL, respectively, and 99mTc‐MIBI scintigraphy showed a hyperfunctioning parathyroid gland. Electromyography revealed myopathic features in the posterior neck extensor muscles. Primary hyperparathyroidism (PHPT)‐associated myopathy was diagnosed as the cause of the DHS. Oral administration of evocalcet ameliorated DHS and normalized the elevated serum calcium levels, whereas iPTH levels remained elevated. Subsequently, parathyroidectomy reduced the iPTH level to normal, and DHS did not flare‐up. Cases of PHPT with DHS as the initial symptom are extremely rare, and to our knowledge, this is the first report of remission of DHS with evocalcet. Therefore, serum iPTH levels may not necessarily correlate with muscle weakness.
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CiteScore
0.80
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