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Tc-sestamibi 显像下表现为无功能性甲状旁腺腺瘤的食管神经鞘瘤:病例报告。

Esophageal schwannoma mimicking non-functional parathyroid adenoma on Tc-sestamibi imaging: a case report.

机构信息

Service of Endocrinology, Diabetology and Metabolism, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.

Service of Otolaryngology and Head and Neck Surgery, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.

出版信息

Front Endocrinol (Lausanne). 2024 May 22;15:1258233. doi: 10.3389/fendo.2024.1258233. eCollection 2024.

Abstract

Technetium-99m sestamibi single-photon emission computed tomography/computed tomography (Tc-sestamibi SPECT/CT) is a mainstay of the pre-operative localization of parathyroid lesions. We report here the case of a 30 year-old woman with a fortuitously discovered 2 cm cervical mass for which a parathyroid origin was originally suspected due to its retro-thyroidal localization and a personal history of nephrolithiasis. Normal serum calcium and parathyroid hormone (PTH) levels excluded primary hyperparathyroidism, raising suspicion of a non-functional parathyroid adenoma, and SPECT/CT imaging showed that the mass was Tc-sestamibi-avid. Fine-needle aspiration (FNA) was performed; cytology was non-diagnostic but the needle washout was negative for thyroglobulin, calcitonin and PTH, arguing against a thyroidal or parathyroidal origin of the mass. Core needle biopsy revealed a schwannoma, ostensibly originating from the recurrent laryngeal nerve; upon surgical resection, it was finally found to arise from the esophageal submucosa. This case illustrates the fact that endocrinologists, radiologists, nuclear medicine, head and neck, and other specialists investigating patients with cervical masses should be aware that schwannomas need to be considered in the differential diagnosis of focal Tc-sestamibi uptake in the neck region.

摘要

锝-99m 甲氧基异丁基异腈单光子发射计算机断层扫描/计算机断层扫描(Tc-甲氧基异丁基异腈 SPECT/CT)是甲状旁腺病变术前定位的主要手段。我们在此报告一例 30 岁女性,偶然发现 2 厘米颈肿块,因其位于甲状腺后而最初怀疑为甲状旁腺起源,并伴有肾结石病史。正常血清钙和甲状旁腺激素(PTH)水平排除了原发性甲状旁腺功能亢进,提示为无功能性甲状旁腺腺瘤,SPECT/CT 成像显示该肿块摄取 Tc-甲氧基异丁基异腈。进行了细针抽吸(FNA);细胞学检查无诊断意义,但针吸冲洗液甲状腺球蛋白、降钙素和 PTH 均为阴性,排除了甲状腺或甲状旁腺起源的肿块。芯针活检显示为神经鞘瘤,显然源自喉返神经;手术切除后,最终发现其源自食管黏膜下层。本例说明,内分泌科医生、放射科医生、核医学医生、头颈部医生和其他检查颈肿块患者的专家应意识到,在颈部区域 Tc-甲氧基异丁基异腈摄取的局灶性鉴别诊断中需要考虑神经鞘瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7358/11150598/806ced1ce990/fendo-15-1258233-g001.jpg

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