McLuckie Adam, Thornton Sydney B, Andree Robin, O'Neil Scott
Medical School, Edward Via College of Osteopathic Medicine, Blacksburg, USA.
Pathology, Sovah Health - Martinsville Hospital, Martinsville, USA.
Cureus. 2025 Mar 21;17(3):e80961. doi: 10.7759/cureus.80961. eCollection 2025 Mar.
Primary hyperparathyroidism due to parathyroid adenoma with concurrent papillary thyroid carcinoma is rare. Less frequently described is the histological interplay between these pathologies. This report describes the case of a 70-year-old female patient who presented with symptomatic hypercalcemia. Subsequent imaging was indicative of a left inferior lobe parathyroid adenoma and highly suspicious for left inferior lobe thyroid carcinoma. A subtotal thyroidectomy with isolated parathyroidectomy was performed. Postoperatively, the patient demonstrated normalization of calcium levels, parathyroid hormone, and resolution of symptoms. Histological evaluation demonstrated direct parathyroid adenoma invasion by the papillary thyroid carcinoma. This report demonstrates that although rare, parathyroid adenoma and papillary thyroid carcinoma can coexist and have the potential to complicate management.
由甲状旁腺腺瘤并发乳头状甲状腺癌引起的原发性甲状旁腺功能亢进症较为罕见。这些病理状况之间的组织学相互作用较少被描述。本报告描述了一名70岁女性患者的病例,该患者出现有症状的高钙血症。随后的影像学检查显示左叶下甲状旁腺腺瘤,并高度怀疑左叶下甲状腺癌。进行了甲状腺次全切除术并单独切除甲状旁腺。术后,患者的钙水平、甲状旁腺激素恢复正常,症状缓解。组织学评估显示乳头状甲状腺癌直接侵犯甲状旁腺腺瘤。本报告表明,尽管罕见,但甲状旁腺腺瘤和乳头状甲状腺癌可同时存在,并有可能使治疗复杂化。