Park S T, Condemi G, Shakir K M, Larson D, Miller D, Ghosh B C
Department of General Surgery, Gyeong-Sang National University Hospital, Korea.
Mil Med. 1998 Apr;163(4):246-9.
Parathyroid carcinoma is a rare endocrine malignancy characterized by the exaggerated metabolic effects of the parathyroid glands. The preoperative differential diagnosis between parathyroid carcinoma and primary hyperparathyroidism is often difficult because many of the signs and symptoms are very similar. Intraoperative differentiation is obscured by the strict anatomic and histologic criteria required for diagnosis of parathyroid carcinoma. We have encountered three patients with parathyroid carcinoma during the last 10 years and managed them successfully. Two of them presented with recurrence of hypercalcemia, one 11 years after and the other 3 years after the primary operation for hyperparathyroidism; both patients were eventually diagnosed with parathyroid carcinoma. The third case was suspected as primary hyperparathyroidism preoperatively but confirmed as carcinoma subsequent to histologic examination.
甲状旁腺癌是一种罕见的内分泌恶性肿瘤,其特征是甲状旁腺的代谢作用过度。甲状旁腺癌与原发性甲状旁腺功能亢进的术前鉴别诊断通常很困难,因为许多体征和症状非常相似。甲状旁腺癌诊断所需的严格解剖学和组织学标准使得术中鉴别变得模糊不清。在过去10年中,我们遇到了3例甲状旁腺癌患者,并成功地对他们进行了治疗。其中2例出现高钙血症复发,1例在原发性甲状旁腺功能亢进手术11年后,另1例在3年后;这2例患者最终均被诊断为甲状旁腺癌。第3例术前怀疑为原发性甲状旁腺功能亢进,但组织学检查后确诊为癌。