Retropharyngeal Ectopic Parathyroid Adenoma Localized by 18F-Fluorocholine Positron Emission Tomography/Computed Tomography: A Case Report.

Q2 Medicine
Journal of Bone Metabolism Pub Date : 2022-08-01 Epub Date: 2022-08-31 DOI:10.11005/jbm.2022.29.3.197
Hyeokjoo Jang, Seunghyun Lee, Dahee Kim, Namki Hong
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Abstract

Ectopic parathyroid adenomas of the retropharyngeal space are relatively rare. Herein, we report a case of primary hyperparathyroidism (PHPT) secondary to a retropharyngeal parathyroid adenoma. A 22-year-old woman presented with elevated serum calcium and parathyroid hormone (PTH) levels, revealed during a medical check-up. The patient had a history of ureteral stones and a confirmed low bone mass. Neck 99mTechnetium-sestamibi singlephoton emission computed tomography (CT) and ultrasonography did not reveal any suspicious lesions. There was no evidence of hereditary PHPT based on the results of targeted gene sequencing. Surgical exploration was unsuccessful, and the PHPT persisted after the first surgery. Approximately a year after the failed operation, 18F-fluorocholine (FCH) positron emission tomography/CT (PET-CT) became available, and when performed, it revealed increased uptake in the retropharyngeal space of the right side of the neck. The results of parathyroid venous sampling were concordant with a >2-fold elevation of PTH level in the veins on the right side of the neck compared to the peripheral veins. The 1.8 cm-diameter mass was successfully removed resulting in an 87% reduction in intraoperative PTH level (198.0-26.5 pg/mL). Subsequently, normalizations of calcium and PTH levels were achieved. In summary, ectopic parathyroid adenomas, including retropharyngeal lesions, should also be suspected when investigating an elusive case of PHPT. 18F-FCH PET-CT can be a useful complementary modality for detecting culprit lesions.

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经18f -氟胆碱正电子发射断层扫描/计算机断层扫描定位的咽后异位甲状旁腺瘤1例报告。
异位甲状旁腺腺瘤在咽后间隙是比较少见的。在此,我们报告一个原发性甲状旁腺功能亢进(PHPT)继发于咽后甲状旁腺瘤的病例。一位22岁的女性在医学检查中发现血清钙和甲状旁腺激素(PTH)水平升高。患者有输尿管结石病史,骨量低。颈部99mtechneium -sestamibi单光子发射计算机断层扫描(CT)和超声检查未发现任何可疑病变。根据靶向基因测序结果,没有证据表明遗传性PHPT。手术探查不成功,第一次手术后PHPT持续存在。手术失败大约一年后,18f -氟胆碱(FCH)正电子发射断层扫描/CT (PET-CT)可用,在执行时,它显示颈部右侧咽后间隙摄取增加。甲状旁腺静脉取样结果与颈部右侧静脉中PTH水平较周围静脉升高>2倍一致。1.8 cm直径的肿块被成功切除,术中PTH水平降低87% (198.0-26.5 pg/mL)。随后,钙和甲状旁腺激素水平恢复正常。总之,异位甲状旁腺瘤,包括咽后病变,在调查难以捉摸的PHPT病例时也应加以怀疑。18F-FCH PET-CT可以作为一种有用的辅助方式来检测罪魁祸首病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Bone Metabolism
Journal of Bone Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
3.70
自引率
0.00%
发文量
23
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