Suppr超能文献

甲状腺髓样癌的一种不寻常表现。

An unusual presentation of medullary thyroid carcinoma.

作者信息

Das Sudip Kr, Varshney Himanshu, Saha M L, Sen Shubhrakanti, Maity Amit Bikram, Paul Ranjan

机构信息

Department of Otorhinolaryngology, BSMC & H, Bankura, 722102 India ; 8, Manik Bandhyopadhyay sarani, Kolkata, 700040 India.

Department of Otorhinolaryngology, Institute of Postgraduate Medical Education & Research (IPGME&R), 244B, Acharya J. C. Bose Road, Kolkata, 700020 India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2013 Jul;65(Suppl 1):195-8. doi: 10.1007/s12070-013-0624-z. Epub 2013 Feb 21.

Abstract

Medullary thyroid carcinoma (MTC) is extremely uncommon having varied presentations & their prognosis is not exactly known; but as MTC is an aggressive tumor hence it needs to be documented in literature to help to know the behaviour of this variant. We report a rare presentation of medullary carcinoma of thyroid in a 48 years old man who presented with huge swelling at left side of neck extending from parotid to supraclavicular region with normal-sized thyroid gland of long duration. FNAC & incision HPE of this swelling was inconclusive so we had operated this swelling. Immunohistochemistry reported it as metastatic Medullary carcinoma of thyroid; tumor cells express Cytokeratin, Calcitonin, EMA, Synaptophysin, Chromogranin-A. The stroma shows deposits of Amyloid, which have been confirmed by Congo red staining. Post-operatively FNAC from thyroid gland supported the diagnosis of Medullary carcinoma. Post-operatively the residual mass was regressed with chemotherapy & radiotherapy. The calcitonin level also decreased following this treatment. There was no recurrence at 11 months but ultimately patient died with metastasis.

摘要

甲状腺髓样癌(MTC)极为罕见,临床表现多样,其预后尚不完全清楚;但由于MTC是一种侵袭性肿瘤,因此需要在文献中记录,以帮助了解这种变体的行为。我们报告了一例48岁男性甲状腺髓样癌的罕见表现,该患者颈部左侧出现巨大肿块,从腮腺延伸至锁骨上区域,甲状腺大小正常,病程较长。该肿块的细针穿刺活检(FNAC)及切开组织病理学检查(HPE)结果不明确,因此我们对该肿块进行了手术。免疫组织化学报告其为甲状腺转移性髓样癌;肿瘤细胞表达细胞角蛋白、降钙素、上皮膜抗原(EMA)、突触素、嗜铬粒蛋白A。间质显示淀粉样物质沉积,经刚果红染色证实。术后甲状腺的FNAC支持髓样癌的诊断。术后残余肿块经化疗和放疗后消退。治疗后降钙素水平也下降。11个月时无复发,但最终患者因转移死亡。

相似文献

1
An unusual presentation of medullary thyroid carcinoma.甲状腺髓样癌的一种不寻常表现。
Indian J Otolaryngol Head Neck Surg. 2013 Jul;65(Suppl 1):195-8. doi: 10.1007/s12070-013-0624-z. Epub 2013 Feb 21.
9
Encapsulated cystic papillary variant of medullary carcinoma of thyroid gland.
Endocr Pathol. 2002 Summer;13(2):167-71. doi: 10.1385/ep:13:2:167.

本文引用的文献

2
Molecular genotyping of medullary thyroid carcinoma can predict tumor recurrence.
Am J Surg Pathol. 2004 Jan;28(1):101-6. doi: 10.1097/00000478-200401000-00012.
5
Cytological aspects of melanotic variant of medullary thyroid carcinoma.甲状腺髓样癌黑色素变异型的细胞学特征
Diagn Cytopathol. 2001 Mar;24(3):206-8. doi: 10.1002/1097-0339(200103)24:3<206::aid-dc1042>3.0.co;2-h.
7
Medullary thyroid cancer: multivariate analysis of prognostic factors influencing survival.
Eur J Surg Oncol. 2000 Nov;26(7):686-90. doi: 10.1053/ejso.2000.0981.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验