Neagoe Radu Mircea, Sala Daniela Tatiana, Borda Angela, Mogoantă Carmen Aurelia, Műhlfay Gheorghe
Second Department of General Surgery, Mures Emergency County Hospital, Tirgu Mures, Romania;
Rom J Morphol Embryol. 2014;55(2 Suppl):669-74.
In the last decade, the clinical picture of primary hyperparathyroidism has changed, with the majority of patients being diagnosed while asymptomatic and the "classical" clinical pattern characterized by bone disease, recurrent nephrolithiasis, peptic ulcer disease, neurological or psychiatric disorders being rarely encountered. In this context, most patients have minimal hypercalcemia and small parathyroid adenomas. Not surprisingly, giant parathyroid adenomas have seldom been described in the literature. We herein report three cases of giant parathyroid adenomas weighing more than 30 g and discuss their clinicopathological and therapeutic particularities. We also review the relevant literature, with the principal aim of outlining the rarity of these giant parathyroid adenomas and the issues concerning their diagnosis and treatment.
在过去十年中,原发性甲状旁腺功能亢进的临床表现发生了变化,大多数患者在无症状时被诊断出来,而以骨病、复发性肾结石、消化性溃疡病、神经或精神障碍为特征的“经典”临床模式很少见。在这种情况下,大多数患者血钙轻度升高,甲状旁腺腺瘤较小。毫不奇怪,文献中很少描述巨大甲状旁腺腺瘤。我们在此报告三例重量超过30克的巨大甲状旁腺腺瘤病例,并讨论其临床病理和治疗特点。我们还回顾了相关文献,主要目的是概述这些巨大甲状旁腺腺瘤的罕见性以及有关其诊断和治疗的问题。