A rare case of poorly differentiated thyroid carcinoma probably arising from a nodular goiter.

Q2 Medicine
BMC Clinical Pathology Pub Date : 2017-06-02 eCollection Date: 2017-01-01 DOI:10.1186/s12907-017-0048-x
Hironao Yasuoka, Yasushi Nakamura, Mitsuyoshi Hirokawa, Ken-Ichi Yoshida, Kana Anno, Masayuki Tori, Masahiko Tsujimoto
{"title":"A rare case of poorly differentiated thyroid carcinoma probably arising from a nodular goiter.","authors":"Hironao Yasuoka,&nbsp;Yasushi Nakamura,&nbsp;Mitsuyoshi Hirokawa,&nbsp;Ken-Ichi Yoshida,&nbsp;Kana Anno,&nbsp;Masayuki Tori,&nbsp;Masahiko Tsujimoto","doi":"10.1186/s12907-017-0048-x","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Some poorly differentiated thyroid carcinomas (PDTC) arise from pre-existing, well-differentiated carcinomas of follicular cell origin; however, others most likely arise de novo<i>.</i> The case of a PDTC adjacent to a pre-existing nodular goiter is very rare.</p><p><strong>Case presentation: </strong>A patient had a PDTC, a widely invasive, cellular tumor with cells that lacked the nuclear features of a papillary thyroid carcinoma. Carcinoma cells were arranged in trabecular, solid, and microfollicular histological patterns and displayed high mitotic activity. A nodule partially encapsulated in a thick fibrous capsule was found adjacent to the PDTC. The nodule was composed of small or dilated follicles, without papillary carcinoma-like nuclear features, that were consistent with a nodular goiter. The PDTC showed a high Ki-67 labeling index and an <i>NRAS</i> gene mutation (codon 61, Q61K).</p><p><strong>Conclusion: </strong>These results support our diagnosis of a PDTC, probably arising from a nodular goiter.</p>","PeriodicalId":35804,"journal":{"name":"BMC Clinical Pathology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2017-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12907-017-0048-x","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Clinical Pathology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s12907-017-0048-x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2017/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 5

Abstract

Background: Some poorly differentiated thyroid carcinomas (PDTC) arise from pre-existing, well-differentiated carcinomas of follicular cell origin; however, others most likely arise de novo. The case of a PDTC adjacent to a pre-existing nodular goiter is very rare.

Case presentation: A patient had a PDTC, a widely invasive, cellular tumor with cells that lacked the nuclear features of a papillary thyroid carcinoma. Carcinoma cells were arranged in trabecular, solid, and microfollicular histological patterns and displayed high mitotic activity. A nodule partially encapsulated in a thick fibrous capsule was found adjacent to the PDTC. The nodule was composed of small or dilated follicles, without papillary carcinoma-like nuclear features, that were consistent with a nodular goiter. The PDTC showed a high Ki-67 labeling index and an NRAS gene mutation (codon 61, Q61K).

Conclusion: These results support our diagnosis of a PDTC, probably arising from a nodular goiter.

Abstract Image

Abstract Image

Abstract Image

一例罕见的低分化甲状腺癌,可能由结节性甲状腺肿引起。
背景:一些低分化甲状腺癌(PDTC)起源于先前存在的滤泡细胞来源的高分化癌;然而,其他的很可能是从头开始的。PDTC与已存在的结节性甲状腺肿相邻是非常罕见的。病例介绍:1例患者患甲状腺乳头状癌(PDTC),这是一种广泛浸润的细胞肿瘤,其细胞缺乏甲状腺乳头状癌的核特征。癌细胞呈小梁状、实体状和微滤泡状排列,有丝分裂活性高。在PDTC附近发现部分包被厚纤维囊的结节。结节由小的或扩张的卵泡组成,无乳头状癌样核征,符合结节性甲状腺肿。PDTC具有较高的Ki-67标记指数和NRAS基因突变(密码子61,Q61K)。结论:这些结果支持我们的诊断PDTC,可能由结节性甲状腺肿引起。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
BMC Clinical Pathology
BMC Clinical Pathology Medicine-Pathology and Forensic Medicine
CiteScore
3.30
自引率
0.00%
发文量
0
期刊介绍: BMC Clinical Pathology is an open access journal publishing original peer-reviewed research articles in all aspects of histopathology, haematology, clinical biochemistry, and medical microbiology (including virology, parasitology, and infection control). BMC Clinical Pathology (ISSN 1472-6890) is indexed/tracked/covered by PubMed, CAS, EMBASE, Scopus and Google Scholar.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信