Fernandez-Ranvier Gustavo G, Jensen Kristin, Khanafshar Elham, Quivey Jeanne M, Glastonbury Christine, Kebebew Electron, Duh Quan-Yang, Clark Orlo H
Department of Surgery, University of California, San Francisco, California, USA.
Endocr Pract. 2007 Nov-Dec;13(7):750-7. doi: 10.4158/EP.13.7.750.
To report a case of nonfunctioning parathyroid carcinoma that was incidentally found during a thyroidectomy for multinodular goiter.
We present a case report, detailing the clinical course and histologic findings in a patient with a nonfunctional parathyroid carcinoma. The related literature is also reviewed.
A 67-year-old woman presented with a 30-year history of a multinodular goiter that was symptomatic. A total thyroidectomy was performed. Histologic examination revealed not only a multinodular thyroid but also a mass in the left lobe, which was diagnostic of a parathyroid carcinoma. Serum calcium and parathyroid hormone levels were normal postoperatively. Eleven months after the initial operation, a suprasternal mass developed, and she underwent neck reexploration and subtotal resection of an invasive recurrent nonfunctioning parathyroid carcinoma. The serum parathyroid hormone and calcium levels were normal before and after the operation. Postoperatively, the patient underwent radiation therapy. Twenty-three months after the initial operation, a computed tomographic scan of the chest revealed an interval increase in size of a nodule in the left lower lobe of the lung, and 30 months after her initial operation, she underwent resection of an isolated, 1-cm (greatest diameter), metastatic parathyroid carcinoma in the left lower lobe of the lung. The patient is currently doing well without evidence of recurrent disease.
Nonfunctioning parathyroid carcinomas are difficult to diagnose and to treat. Recurrent disease after operation is common, and radiation therapy may help stabilize tumor growth. Patients with nonfunctioning parathyroid carcinomas appear to have a poorer prognosis than do those with functioning parathyroid cancers.
报告1例在因多结节性甲状腺肿行甲状腺切除术时偶然发现的无功能甲状旁腺癌病例。
我们呈现1例病例报告,详细描述1例无功能甲状旁腺癌患者的临床病程及组织学检查结果。同时对相关文献进行回顾。
1名67岁女性,有30年有症状的多结节性甲状腺肿病史。行全甲状腺切除术。组织学检查不仅发现多结节性甲状腺,还在左叶发现1个肿块,诊断为甲状旁腺癌。术后血清钙和甲状旁腺激素水平正常。初次手术后11个月,出现胸骨上肿块,她接受了颈部再次探查及侵袭性复发性无功能甲状旁腺癌的次全切除术。手术前后血清甲状旁腺激素和钙水平均正常。术后患者接受了放射治疗。初次手术后23个月,胸部计算机断层扫描显示左肺下叶1个结节大小较前增大,初次手术后30个月,她接受了左肺下叶1个孤立的、直径1 cm(最大径)的转移性甲状旁腺癌切除术。患者目前情况良好,无疾病复发迹象。
无功能甲状旁腺癌难以诊断和治疗。术后复发很常见,放射治疗可能有助于稳定肿瘤生长。无功能甲状旁腺癌患者的预后似乎比有功能甲状旁腺癌患者更差。