Çetin Kenan, Sıkar Hasan E, Temizkan Şule, Ofluoğlu Cem B, Özderya Ayşenur, Aydın Kadriye, Gül Aylin E, Küçük Hasan F
Department of General Surgery, University of Health Sciences, Kartal Dr. Lutfi Kirdar Training and Research Hospital, 34890, Istanbul, Turkey.
Department of Endocrinology, Faculty of Medicine, Yeditepe University, Istanbul, Turkey.
World J Surg. 2019 May;43(5):1243-1248. doi: 10.1007/s00268-019-04920-4.
To investigate the relationship between primary hyperparathyroidism (pHPT) and papillary thyroid cancer (PTC).
The perioperative findings of 275 patients with pHPT who underwent surgery between January 2014 and December 2017 were retrospectively reviewed. Thirty-one patients were diagnosed with pHPT and PTC concurrently. Pathology results and demographic findings of these patients were compared with 186 patients who underwent thyroidectomy and diagnosed with PTC at the same time interval.
The co-occurrence of pHPT and PTC was 11.3% (31/275). The median ages of the pHPT, pHPT + PTC, and PTC groups were 55, 57, and 50 years old, respectively (p < 0.001). The diameter of tumor was smaller in the pHPT + PTC group [median 7 mm (range 0.5-25 mm) vs. 15 mm (range 1-100 mm)], with higher rates of microcarcinomas (p < 0.001), than the patients in the PTC group. Examination of tumor morphology showed higher rates of tumor capsule invasion and multicentricity in the pHPT + PTC group than those in the isolated PTC group (p = 0.02, p = 0.04, respectively).
The pHPT + PTC group had significantly smaller tumor diameter than the PTC group. This result may support the idea that pHPT leads to overdiagnosis of PTC. However, observation of high rates of tumor capsule invasion and multicentricity in the pHPT + PTC group may suggest an associative etiology with more aggressive PTC.
探讨原发性甲状旁腺功能亢进症(pHPT)与甲状腺乳头状癌(PTC)之间的关系。
回顾性分析2014年1月至2017年12月期间接受手术的275例pHPT患者的围手术期资料。其中31例患者同时诊断为pHPT和PTC。将这些患者的病理结果和人口统计学资料与同期接受甲状腺切除术并诊断为PTC的186例患者进行比较。
pHPT和PTC的共发生率为11.3%(31/275)。pHPT组、pHPT+PTC组和PTC组的中位年龄分别为55岁、57岁和50岁(p<0.001)。pHPT+PTC组的肿瘤直径较小[中位值7mm(范围0.5-25mm)vs.15mm(范围1-100mm)],微癌发生率较高(p<0.001)。肿瘤形态学检查显示,pHPT+PTC组的肿瘤包膜侵犯率和多中心发生率高于单纯PTC组(分别为p=0.02,p=0.04)。
pHPT+PTC组的肿瘤直径明显小于PTC组。这一结果可能支持pHPT导致PTC过度诊断的观点。然而,pHPT+PTC组肿瘤包膜侵犯率和多中心发生率较高,可能提示与侵袭性更强的PTC存在关联病因。