Inherited thyroid tumours
Inherited thyroid tumours are an important group which need clarification. This is partly because of the common use of the term Familial Non-Medullary Thyroid Cancer when some of the specific entities included under this heading really represent inherited benign tumours with a risk of progression to...
Gespeichert in:
Veröffentlicht in: | Endocrine 2020-05, Vol.68 (2), p.271-273 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 273 |
---|---|
container_issue | 2 |
container_start_page | 271 |
container_title | Endocrine |
container_volume | 68 |
creator | Williams, Dillwyn |
description | Inherited thyroid tumours are an important group which need clarification. This is partly because of the common use of the term Familial Non-Medullary Thyroid Cancer when some of the specific entities included under this heading really represent inherited benign tumours with a risk of progression to malignancy. The subject is briefly reviewed, and one syndromic and one non-syndromic type of inherited thyroid tumours of follicular cell origin discussed in more detail to emphasise the point that each of these groups need to be treated as separate entities. |
doi_str_mv | 10.1007/s12020-020-02252-1 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2379019053</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2408866842</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-182d28b8bea53b6680d7fc5e8f9f54fdf9eaf00535d4db5f8c4bbfe35dff00593</originalsourceid><addsrcrecordid>eNp9kE1LAzEQhoMotlZ_gB5E8OIlOkk23eQoxY9CwYuCt7DZJHZLd7cmu4f-e6dsVfAgZJgk88w7w0vIBYNbBpDfJcaBAx2CS07ZARkzKTUFrB_iXUhJAdT7iJyktAKk-DQ_JiPBmdJ4xuR83ix9rDrvrrrlNrYV5r5u-5hOyVEo1smf7fOEvD0-vM6e6eLlaT67X9BS5LKjTHHHlVXWF1LY6VSBy0MpvQo6yCy4oH0RAKSQLnNWBlVm1gaPz7D71mJCbgbdTWw_e586U1ep9Ot10fi2T4aLXAPTqIDo9R90hZs2uJ3hGSiF0zOOFB-oMrYpRR_MJlZ1EbeGgdkZZwbjzBBonGHYdLmX7m3t3U_Lt1MIiAFIWGo-fPyd_Y_sFz4Zdwc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2408866842</pqid></control><display><type>article</type><title>Inherited thyroid tumours</title><source>Springer Nature - Complete Springer Journals</source><creator>Williams, Dillwyn</creator><creatorcontrib>Williams, Dillwyn</creatorcontrib><description>Inherited thyroid tumours are an important group which need clarification. This is partly because of the common use of the term Familial Non-Medullary Thyroid Cancer when some of the specific entities included under this heading really represent inherited benign tumours with a risk of progression to malignancy. The subject is briefly reviewed, and one syndromic and one non-syndromic type of inherited thyroid tumours of follicular cell origin discussed in more detail to emphasise the point that each of these groups need to be treated as separate entities.</description><identifier>ISSN: 1355-008X</identifier><identifier>EISSN: 1559-0100</identifier><identifier>DOI: 10.1007/s12020-020-02252-1</identifier><identifier>PMID: 32189189</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Diabetes ; Endocrinology ; Humanities and Social Sciences ; Internal Medicine ; Malignancy ; Medicine ; Medicine & Public Health ; multidisciplinary ; Original Article ; Science ; Thyroid cancer ; Thyroid gland ; Tumors</subject><ispartof>Endocrine, 2020-05, Vol.68 (2), p.271-273</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020</rights><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-182d28b8bea53b6680d7fc5e8f9f54fdf9eaf00535d4db5f8c4bbfe35dff00593</citedby><cites>FETCH-LOGICAL-c375t-182d28b8bea53b6680d7fc5e8f9f54fdf9eaf00535d4db5f8c4bbfe35dff00593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12020-020-02252-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12020-020-02252-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32189189$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Williams, Dillwyn</creatorcontrib><title>Inherited thyroid tumours</title><title>Endocrine</title><addtitle>Endocrine</addtitle><addtitle>Endocrine</addtitle><description>Inherited thyroid tumours are an important group which need clarification. This is partly because of the common use of the term Familial Non-Medullary Thyroid Cancer when some of the specific entities included under this heading really represent inherited benign tumours with a risk of progression to malignancy. The subject is briefly reviewed, and one syndromic and one non-syndromic type of inherited thyroid tumours of follicular cell origin discussed in more detail to emphasise the point that each of these groups need to be treated as separate entities.</description><subject>Diabetes</subject><subject>Endocrinology</subject><subject>Humanities and Social Sciences</subject><subject>Internal Medicine</subject><subject>Malignancy</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>multidisciplinary</subject><subject>Original Article</subject><subject>Science</subject><subject>Thyroid cancer</subject><subject>Thyroid gland</subject><subject>Tumors</subject><issn>1355-008X</issn><issn>1559-0100</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMotlZ_gB5E8OIlOkk23eQoxY9CwYuCt7DZJHZLd7cmu4f-e6dsVfAgZJgk88w7w0vIBYNbBpDfJcaBAx2CS07ZARkzKTUFrB_iXUhJAdT7iJyktAKk-DQ_JiPBmdJ4xuR83ix9rDrvrrrlNrYV5r5u-5hOyVEo1smf7fOEvD0-vM6e6eLlaT67X9BS5LKjTHHHlVXWF1LY6VSBy0MpvQo6yCy4oH0RAKSQLnNWBlVm1gaPz7D71mJCbgbdTWw_e586U1ep9Ot10fi2T4aLXAPTqIDo9R90hZs2uJ3hGSiF0zOOFB-oMrYpRR_MJlZ1EbeGgdkZZwbjzBBonGHYdLmX7m3t3U_Lt1MIiAFIWGo-fPyd_Y_sFz4Zdwc</recordid><startdate>20200501</startdate><enddate>20200501</enddate><creator>Williams, Dillwyn</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20200501</creationdate><title>Inherited thyroid tumours</title><author>Williams, Dillwyn</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-182d28b8bea53b6680d7fc5e8f9f54fdf9eaf00535d4db5f8c4bbfe35dff00593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Diabetes</topic><topic>Endocrinology</topic><topic>Humanities and Social Sciences</topic><topic>Internal Medicine</topic><topic>Malignancy</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>multidisciplinary</topic><topic>Original Article</topic><topic>Science</topic><topic>Thyroid cancer</topic><topic>Thyroid gland</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Williams, Dillwyn</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Endocrine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Williams, Dillwyn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inherited thyroid tumours</atitle><jtitle>Endocrine</jtitle><stitle>Endocrine</stitle><addtitle>Endocrine</addtitle><date>2020-05-01</date><risdate>2020</risdate><volume>68</volume><issue>2</issue><spage>271</spage><epage>273</epage><pages>271-273</pages><issn>1355-008X</issn><eissn>1559-0100</eissn><abstract>Inherited thyroid tumours are an important group which need clarification. This is partly because of the common use of the term Familial Non-Medullary Thyroid Cancer when some of the specific entities included under this heading really represent inherited benign tumours with a risk of progression to malignancy. The subject is briefly reviewed, and one syndromic and one non-syndromic type of inherited thyroid tumours of follicular cell origin discussed in more detail to emphasise the point that each of these groups need to be treated as separate entities.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>32189189</pmid><doi>10.1007/s12020-020-02252-1</doi><tpages>3</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1355-008X |
ispartof | Endocrine, 2020-05, Vol.68 (2), p.271-273 |
issn | 1355-008X 1559-0100 |
language | eng |
recordid | cdi_proquest_miscellaneous_2379019053 |
source | Springer Nature - Complete Springer Journals |
subjects | Diabetes Endocrinology Humanities and Social Sciences Internal Medicine Malignancy Medicine Medicine & Public Health multidisciplinary Original Article Science Thyroid cancer Thyroid gland Tumors |
title | Inherited thyroid tumours |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T02%3A11%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Inherited%20thyroid%20tumours&rft.jtitle=Endocrine&rft.au=Williams,%20Dillwyn&rft.date=2020-05-01&rft.volume=68&rft.issue=2&rft.spage=271&rft.epage=273&rft.pages=271-273&rft.issn=1355-008X&rft.eissn=1559-0100&rft_id=info:doi/10.1007/s12020-020-02252-1&rft_dat=%3Cproquest_cross%3E2408866842%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2408866842&rft_id=info:pmid/32189189&rfr_iscdi=true |