McClenaghan Fiona, Qureshi Yassar A
Department of Surgery, the Royal London Hospital, London, UK.
Gland Surg. 2015 Aug;4(4):329-38. doi: 10.3978/j.issn.2227-684X.2015.05.09.
Parathyroid carcinoma is an exceedingly rare endocrine malignancy first described in 1933. It accounts for between 0.5% and 5% of all cases of primary hyperparathyroidism. Parathyroid carcinoma is unusual among endocrine malignancies, being more hormonally active than its benign counterpart. Parathyroid carcinoma poses a diagnostic challenge both clinically and histologically due to the lack of features which can definitively distinguish malignant from benign disease early in its clinical course. Here, we describe the clinical features of the disease, and present the current opinion on optimal management. Further, we analyse the most recent histological advances made to aid in the diagnosis and management of this rare, but potentially devastating, disease.
甲状旁腺癌是一种极其罕见的内分泌恶性肿瘤,于1933年首次被描述。它占所有原发性甲状旁腺功能亢进病例的0.5%至5%。甲状旁腺癌在内分泌恶性肿瘤中较为特殊,其激素活性比良性对应物更强。由于在临床病程早期缺乏能够明确区分恶性与良性疾病的特征,甲状旁腺癌在临床和组织学上都带来了诊断挑战。在此,我们描述该疾病的临床特征,并阐述当前关于最佳治疗的观点。此外,我们分析了为辅助诊断和治疗这种罕见但可能具有毁灭性的疾病所取得的最新组织学进展。