Incidental synchronous intrathyroidal parathyroid carcinomas and papillary thyroid microcarcinoma with compressive neck mass and primary hyperparathyroidism: case report and literature review.

IF 2.8 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Tianfeng Xu, Xun Zheng, Tao Wei
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引用次数: 0

Abstract

Background: Parathyroid carcinoma (PC) is a rare malignancy, often diagnosed incidentally through postoperative pathological examination. The occurrence of nodular goiter, intrathyroidal parathyroid carcinoma, contralateral parathyroid adenoma (PA), and papillary thyroid microcarcinoma (PTMC) is extremely uncommon, which prompted us to report our case experience.

Case presentation: We describe a 67-year-old male who presented with a cervical mass causing tracheal compression, which prompted him to seek medical advice. Based on preoperative auxiliary examination results from color Doppler ultrasound, SPECT parathyroid imaging, and blood tests, he was initially diagnosed with a suspected parathyroid adenoma and nodular goiter. Excision of the right lobe and isthmus of the thyroid, and left superior parathyroid gland was conducted, which were sent to intraoperative frozen pathological examination. During intraoperative observation, adhesion around the right thyroid lobe was discovered. Consequently, right central area lymph node dissection was performed due to suspicion of an aggressive malignant tumor. Histology and immunohistochemistry analysis revealed incidental intrathyroidal parathyroid carcinoma, contralateral parathyroid adenoma, classical papillary thyroid microcarcinoma, and nodular goiter.

Conclusion: Parathyroid carcinoma should be highly suspected when extremely high levels of PTH and severe hypercalcemia are present, which cannot be simply explained by a preoperatively localized parathyroid adenoma, especially when suspicious malignant adhesion is found during intraoperative exploration. In cases where multifocal thyroid nodules are associated with increased uptake of 99Tc-sestamibi, the possibility of coexisting carcinomas should be considered, not only for thyroid malignancy but also for the potential presence of intrathyroidal parathyroid carcinoma.

偶发同步甲状旁腺内癌和甲状腺乳头状微癌伴压迫性颈部肿块和原发性甲状旁腺功能亢进症:病例报告和文献综述。
背景:甲状旁腺癌(PC)是一种罕见的恶性肿瘤:甲状旁腺癌(PC)是一种罕见的恶性肿瘤,通常通过术后病理检查偶然确诊。结节性甲状腺肿、甲状旁腺内癌、对侧甲状旁腺腺瘤(PA)和甲状腺乳头状微癌(PTMC)的发生率极低,这促使我们报告我们的病例经历:我们描述了一名67岁的男性患者,他因颈部肿块压迫气管而就医。根据彩色多普勒超声、SPECT甲状旁腺成像和血液检查的术前辅助检查结果,他被初步诊断为疑似甲状旁腺腺瘤和结节性甲状腺肿。手术切除了甲状腺右叶、峡部和左侧甲状旁腺上叶,并送往术中冰冻病理检查。术中观察发现,右侧甲状腺叶周围有粘连。因此,因怀疑是侵袭性恶性肿瘤而进行了右中央区淋巴结清扫术。组织学和免疫组化分析显示,该患者偶发甲状旁腺内癌、对侧甲状旁腺腺瘤、典型甲状腺乳头状微癌和结节性甲状腺肿:当出现极高的PTH水平和严重的高钙血症时,尤其是术中探查时发现可疑的恶性粘连时,应高度怀疑甲状旁腺癌。在多灶性甲状腺结节伴有99锝-铯同位素摄取增加的病例中,应考虑并存癌的可能性,不仅要考虑甲状腺恶性肿瘤,还要考虑可能存在的甲状旁腺内癌。
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来源期刊
BMC Endocrine Disorders
BMC Endocrine Disorders ENDOCRINOLOGY & METABOLISM-
CiteScore
4.40
自引率
0.00%
发文量
280
审稿时长
>12 weeks
期刊介绍: BMC Endocrine Disorders is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of endocrine disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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