Sivrikoz Emre, Ozbey Nese Colak, Kaya Bulent, Erbil Yesim, Kaya Serkan, Yilmazbayhan Dilek, Firat Pinar, Kapran Yersu
Department of General Surgery, Istanbul University, Istanbul Medical School, Capa-Istanbul 34093, Turkey.
J Med Case Rep. 2012 Feb 27;6:73. doi: 10.1186/1752-1947-6-73.
Autopsy series have shown that metastasis to the thyroid gland has occurred in up to 24% of patients who have died of cancer. Neuroendocrine tumors may metastasize to thyroid gland.
Case 1 was a 17-year-old Turkish woman who was referred from our Endocrinology Department for a thyroidectomy for treatment of neuroendocrine tumor metastasis. She was treated with a bilateral total thyroidectomy. Histopathological examination results were consistent with a neuroendocrine tumor; neoplastic cells showed strong immunoreactivity to chromogranin A and synaptophysin, but the immunohistochemical profile was inconsistent with medullary thyroid carcinoma in that the tumor was negative for calcitonin, carcinoembryonic antigen, and thyroid transcription factor-1.Case 2 was a 54-year-old Turkish woman who presented with a 3-cm nodule on her right thyroid lobe. She had undergone surgery for a right lung mass four years previously. After a right pneumonectomy, thymectomy and lymph node dissection, a typical carcinoid tumor was diagnosed. Under ultrasonographic guidance, fine needle aspiration biopsy of her right thyroid pole nodule was performed and the biopsy was compatible with a neuroendocrine tumor metastasis. She was treated with a bilateral total thyroidectomy. Histopathological examination indicated three nodular lesions, 5 cm and 0.4 cm in diameter in her right lobe and 0.1 cm in diameter in her left lobe. The tumors were consistent with a neuroendocrine phenotype, showing strong immunoreactivity to chromogranin A and synaptophysin.
Thyroid nodules detected during follow-up of neuroendocrine tumor patients should be thoroughly investigated. A fine needle aspiration biopsy of the thyroid confirms the diagnosis in most cases and leads to appropriate management of those patients and may prevent unnecessary treatment approaches.
尸检系列研究表明,死于癌症的患者中,高达24%发生了甲状腺转移。神经内分泌肿瘤可能转移至甲状腺。
病例1是一名17岁的土耳其女性,因神经内分泌肿瘤转移接受甲状腺切除术,从我们的内分泌科转诊而来。她接受了双侧甲状腺全切除术。组织病理学检查结果与神经内分泌肿瘤一致;肿瘤细胞对嗜铬粒蛋白A和突触素呈强免疫反应性,但免疫组化特征与甲状腺髓样癌不一致,因为该肿瘤降钙素、癌胚抗原和甲状腺转录因子-1均为阴性。病例2是一名54岁的土耳其女性,其右甲状腺叶有一个3厘米的结节。四年前她曾因右肺肿块接受手术。在进行右肺切除、胸腺切除和淋巴结清扫后,诊断为典型类癌。在超声引导下,对其右甲状腺极结节进行了细针穿刺活检,活检结果与神经内分泌肿瘤转移相符。她接受了双侧甲状腺全切除术。组织病理学检查显示右叶有三个结节性病变,直径分别为5厘米和0.4厘米,左叶直径为0.1厘米。肿瘤符合神经内分泌表型,对嗜铬粒蛋白A和突触素呈强免疫反应性。
神经内分泌肿瘤患者随访期间发现的甲状腺结节应进行全面检查。甲状腺细针穿刺活检在大多数情况下可确诊,并能对这些患者进行适当管理,还可避免不必要的治疗方法。