Jr., Duke University Medical Center, Durham, North Carolina 27710, USA.
Oncologist. 2010;15(1):61-72. doi: 10.1634/theoncologist.2009-0185. Epub 2010 Jan 5.
Parathyroid carcinoma is an indolent but ultimately life-threatening malignancy. Due to the lack of definitive diagnostic markers and overlapping clinical features of benign primary hyperparathyroidism (PHPT), this disease is often misdiagnosed as parathyroid adenoma. Therefore, a high index of suspicion preoperatively and early intraoperative recognition with en bloc surgical resection are crucial for favorable outcome. Owing to the rarity of the disease, little is known about the molecular pathogenesis of parathyroid carcinoma. Here, we review the literature to present current understanding of the disease and provide new information on gene expression and use of intraoperative parathyroid hormone (PTH) monitoring in the surgical management of this rare malignancy. Specifically, using microarray transcriptome analysis of an unequivocal case of parathyroid carcinoma and a biopsy from the same patient's normal parathyroid gland, we identify APP, CDH1, KCNJ16, and UCHL1 as differentially expressed genes in parathyroid carcinoma. Further, using case records from four cases of unequivocal parathyroid carcinoma, we compared intraoperative PTH kinetics of these patients to 475 patients with benign PHPT, and show that intraoperative PTH monitoring is accurate in predicting postoperative normocalcemia in initial en bloc operations for parathyroid carcinoma.
甲状旁腺癌是一种惰性但最终危及生命的恶性肿瘤。由于缺乏明确的诊断标志物和良性原发性甲状旁腺功能亢进症 (PHPT) 的临床特征重叠,这种疾病经常被误诊为甲状旁腺瘤。因此,术前高度怀疑和术中早期整块切除对于获得良好的结果至关重要。由于这种疾病很少见,因此对甲状旁腺癌的分子发病机制知之甚少。在这里,我们复习文献,介绍对这种罕见恶性肿瘤的当前认识,并提供有关基因表达和术中甲状旁腺激素 (PTH) 监测在这种疾病的手术管理中的新信息。具体来说,我们使用明确的甲状旁腺癌病例和同一患者正常甲状旁腺的活检进行微阵列转录组分析,确定 APP、CDH1、KCNJ16 和 UCHL1 是甲状旁腺癌中差异表达的基因。此外,我们使用四起明确的甲状旁腺癌病例的病历记录,将这些患者的术中 PTH 动力学与 475 名良性 PHPT 患者进行比较,并表明术中 PTH 监测可准确预测甲状旁腺癌初始整块切除术后的术后正常血钙水平。