Intrathyroidal Parathyroid Carcinoma: Case Report and Literature Review.

IF 1 4区 医学 Q3 OTORHINOLARYNGOLOGY Ent-Ear Nose & Throat Journal Pub Date : 2025-01-01 Epub Date: 2022-04-09 DOI:10.1177/01455613221093729
Hannah Daniel, Pranati Pillutla, Cynthia Schwartz, Tam Nguyen
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Abstract

Intrathyroidal parathyroid carcinoma (PC) is a rare malignancy that is usually difficult to diagnose. We present a case of a 31-year-old male with a history of hyperparathyroidism who was found to have intrathyroidal PC upon review of immunostains along with a review of the current literature. A systematic review of the literature utilizing the PubMed database identified 24 relevant, full-text articles. 25 cases were analyzed, including our own report. The case of a 31-year-old man with a history of hyperparathyroidism managed with subtotal thyroidectomy and subtotal parathyroidectomy who had persistent hypercalcemia and elevated parathyroid hormone. Abnormal radiotracer uptake was noted in the left thyroid gland. Neck exploration with left parathyroidectomy and revision thyroidectomy was performed. A candidate left inferior parathyroid was found within the left thyroid lobe remnant and identified as parathyroid carcinoma. Immunostains determined an intrathyroidal parathyroid carcinoma. The literature review shows the average presenting age was 50.9 years. 54.17% (CI, 43-82%) of affected patients are female. Right-sided thyroid involvement is seen in 54.17% (CI, 34-74%) of cases. The inferior aspect of the thyroid is involved in 66.67% of cases (CI, 53-89%). Intrathyroidal parathyroid carcinoma is a rare and challenging diagnosis due to similarities with other more common endocrine abnormalities. This review found that the inferior parathyroid is more likely to be located within the thyroid gland. Surgeons may consider aberrant anatomical locations, including intrathyroidal locations, for the inferior parathyroid glands.

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甲状腺内甲状旁腺癌1例报告及文献复习。
甲状腺内甲状旁腺癌(PC)是一种罕见的恶性肿瘤,通常难以诊断。我们报告了一例有甲状旁腺功能亢进病史的31岁男性病例,在对免疫染色和现有文献进行回顾后,发现其有甲状腺内PC。利用PubMed数据库对文献进行的系统综述确定了24篇相关的全文文章。对25例病例进行了分析,包括我们自己的报告。一例31岁有甲状旁腺功能亢进史的男性患者接受了甲状腺次全切除术和甲状旁腺次全切除手术,并伴有持续性高钙血症和甲状旁腺激素升高。在左侧甲状腺发现放射性示踪剂摄取异常。颈部探查采用左侧甲状旁腺切除术和甲状腺翻修术。在左甲状腺叶残余物内发现了一个候选的左下甲状旁腺,并确定为甲状旁腺癌。免疫染色确定为甲状腺内甲状旁腺癌。文献综述显示,平均发病年龄为50.9岁。54.17%(CI,43-82%)的患者为女性。54.17%(CI,34-74%)的病例可见右侧甲状腺受累。66.67%的病例涉及甲状腺下侧面(CI,53-89%)。甲状腺内甲状旁腺癌是一种罕见且具有挑战性的诊断,因为它与其他更常见的内分泌异常相似。这篇综述发现,下甲状旁腺更有可能位于甲状腺内。外科医生可能会考虑下甲状旁腺的异常解剖位置,包括甲状腺内位置。
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来源期刊
Ent-Ear Nose & Throat Journal
Ent-Ear Nose & Throat Journal 医学-耳鼻喉科学
CiteScore
3.20
自引率
0.00%
发文量
385
审稿时长
6-12 weeks
期刊介绍: Ear, Nose & Throat Journal provides practical, peer-reviewed original clinical articles, highlighting scientific research relevant to clinical care, and case reports that describe unusual entities or innovative approaches to treatment and case management. ENT Journal utilizes multiple channels to deliver authoritative and timely content that informs, engages, and shapes the industry now and into the future.
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