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以甲状腺转移为表现的神经内分泌肿瘤:病例系列

Neuroendocrine tumors presenting with thyroid gland metastasis: a case series.

作者信息

Sivrikoz Emre, Ozbey Nese Colak, Kaya Bulent, Erbil Yesim, Kaya Serkan, Yilmazbayhan Dilek, Firat Pinar, Kapran Yersu

机构信息

Department of General Surgery, Istanbul University, Istanbul Medical School, Capa-Istanbul 34093, Turkey.

出版信息

J Med Case Rep. 2012 Feb 27;6:73. doi: 10.1186/1752-1947-6-73.

Abstract

INTRODUCTION

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 PRESENTATIONS

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.

CONCLUSION

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.

摘要

引言

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。

病例报告

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bab/3311143/8ce500336718/1752-1947-6-73-1.jpg

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