Increased diagnostic sensitivity of palpation‐guided thyroid nodule fine‐needle aspiration cytology by BRAF V600E‐mutation analysis
Papillary thyroid carcinoma (PTC) is the most common type of thyroid cancer and its incidence is increasing. Preoperative diagnosis is warranted in order to avoid ‘two‐stage’ procedures that are associated with additional costs and higher radioactive iodine remnant uptake. In the setting of thyroid...
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description | Papillary thyroid carcinoma (PTC) is the most common type of thyroid cancer and its incidence is increasing. Preoperative diagnosis is warranted in order to avoid ‘two‐stage’ procedures that are associated with additional costs and higher radioactive iodine remnant uptake. In the setting of thyroid cancer, somatic BRAF V600E‐mutations are highly specific for PTC and can be analyzed in aspirates from fine‐needle aspiration cytology (FNAC). The ‘gold standard’ to perform FNAC is ultrasound guidance. Here, we analyze whether adding BRAF V600E‐mutation analysis could be of value in palpation‐guided FNACs. A total of 430 consecutive patients were included. Ultrasound‐guided FNACs were performed in 251 patients and 179 patients underwent palpation‐guided FNACs. BRAF V600E‐mutation analysis was performed using two methods, an allele‐specific polymerase chain reaction (PCR) analyzed by capillary gel electrophoresis (PCR/Qiaxcel), and a droplet digital PCR (ddPCR) assay. A total of 80 patients underwent surgery, and histology revealed 25 patients to have PTC. Of the 25 PTCs, 23 (92%) showed a BRAF V600E‐mutation. Both mutation analysis methods (PCR/Qiaxcel and ddPCR) produced concordant results. In the ultrasound‐guided group, the preoperative diagnostic sensitivity of FNAC using the Bethesda classification alone was very high and additional BRAF V600E‐mutation analysis added little to the preoperative diagnostic sensitivity. By contrast, in the palpation‐guided group, by adding BRAF V600E‐mutation analysis, eight instead of four patients were diagnosed of having PTC. This increase in the diagnostic sensitivity was statistically significant (p |
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Preoperative diagnosis is warranted in order to avoid ‘two‐stage’ procedures that are associated with additional costs and higher radioactive iodine remnant uptake. In the setting of thyroid cancer, somatic BRAF V600E‐mutations are highly specific for PTC and can be analyzed in aspirates from fine‐needle aspiration cytology (FNAC). The ‘gold standard’ to perform FNAC is ultrasound guidance. Here, we analyze whether adding BRAF V600E‐mutation analysis could be of value in palpation‐guided FNACs. A total of 430 consecutive patients were included. Ultrasound‐guided FNACs were performed in 251 patients and 179 patients underwent palpation‐guided FNACs. BRAF V600E‐mutation analysis was performed using two methods, an allele‐specific polymerase chain reaction (PCR) analyzed by capillary gel electrophoresis (PCR/Qiaxcel), and a droplet digital PCR (ddPCR) assay. A total of 80 patients underwent surgery, and histology revealed 25 patients to have PTC. Of the 25 PTCs, 23 (92%) showed a BRAF V600E‐mutation. Both mutation analysis methods (PCR/Qiaxcel and ddPCR) produced concordant results. In the ultrasound‐guided group, the preoperative diagnostic sensitivity of FNAC using the Bethesda classification alone was very high and additional BRAF V600E‐mutation analysis added little to the preoperative diagnostic sensitivity. By contrast, in the palpation‐guided group, by adding BRAF V600E‐mutation analysis, eight instead of four patients were diagnosed of having PTC. This increase in the diagnostic sensitivity was statistically significant (p < 0.05). The costs per sample were as low as 62 USD (PCR/Qiaxcel and ddPCR) and 35 USD (PCR/Qiaxcel only). Ultrasound‐guided FNAC should be aimed for when dealing with thyroid nodules. However, if palpation‐guided FNAC cannot be avoided or may be required due to resource utilization, adding BRAF V600E‐mutation analysis using the methods described in this study might significantly increase the proportion of preoperatively diagnosed PTCs. The additional costs can be considered very reasonable.</description><identifier>ISSN: 2056-4538</identifier><identifier>EISSN: 2056-4538</identifier><identifier>DOI: 10.1002/cjp2.231</identifier><identifier>PMID: 34156770</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Analysis ; Biomarkers, Tumor - genetics ; Biopsy, Fine-Needle ; BRAF ; Capillary electrophoresis ; Cellular biology ; Cytology ; DNA Mutational Analysis ; Enzymes ; fine‐needle aspiration cytology ; FNAC ; Gel electrophoresis ; Gene mutations ; Genetic aspects ; Humans ; Image-Guided Biopsy ; Iodine ; Mutation ; mutation analysis ; Original ; Palpation ; palpation‐guided ; Papillary thyroid carcinoma ; Patients ; Polymerase chain reaction ; Polymorphism ; Predictive Value of Tests ; Proto-Oncogene Proteins B-raf - genetics ; Reproducibility of Results ; Resource utilization ; Statistical analysis ; Thyroid cancer ; Thyroid Cancer, Papillary - epidemiology ; Thyroid Cancer, Papillary - genetics ; Thyroid Cancer, Papillary - pathology ; Thyroid Neoplasms - enzymology ; Thyroid Neoplasms - genetics ; Thyroid Neoplasms - pathology ; Tumors ; Ultrasonic imaging ; Ultrasonography ; Ultrasound ; ultrasound‐guided</subject><ispartof>The Journal of Pathology: Clinical Research, 2021-11, Vol.7 (6), p.556-564</ispartof><rights>2021 The Authors. published by The Pathological Society of Great Britain and Ireland & John Wiley & Sons, Ltd.</rights><rights>2021 The Authors. The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland & John Wiley & Sons, Ltd.</rights><rights>COPYRIGHT 2021 John Wiley & Sons, Inc.</rights><rights>2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6091-b0be83f12c6fd957ff1d7f90e6c917c942cd6bb09903e440f605e358799401c53</citedby><cites>FETCH-LOGICAL-c6091-b0be83f12c6fd957ff1d7f90e6c917c942cd6bb09903e440f605e358799401c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8503891/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8503891/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,552,727,780,784,864,885,1417,2102,11562,27924,27925,45574,45575,46052,46476,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34156770$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-180109$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Gimm, Oliver</creatorcontrib><creatorcontrib>Ivansson, Kristin</creatorcontrib><creatorcontrib>Beka, Ervin</creatorcontrib><creatorcontrib>Rossitti, Hugo M</creatorcontrib><creatorcontrib>Garvin, Stina</creatorcontrib><creatorcontrib>Söderkvist, Peter</creatorcontrib><title>Increased diagnostic sensitivity of palpation‐guided thyroid nodule fine‐needle aspiration cytology by BRAF V600E‐mutation analysis</title><title>The Journal of Pathology: Clinical Research</title><addtitle>J Pathol Clin Res</addtitle><description>Papillary thyroid carcinoma (PTC) is the most common type of thyroid cancer and its incidence is increasing. Preoperative diagnosis is warranted in order to avoid ‘two‐stage’ procedures that are associated with additional costs and higher radioactive iodine remnant uptake. In the setting of thyroid cancer, somatic BRAF V600E‐mutations are highly specific for PTC and can be analyzed in aspirates from fine‐needle aspiration cytology (FNAC). The ‘gold standard’ to perform FNAC is ultrasound guidance. Here, we analyze whether adding BRAF V600E‐mutation analysis could be of value in palpation‐guided FNACs. A total of 430 consecutive patients were included. Ultrasound‐guided FNACs were performed in 251 patients and 179 patients underwent palpation‐guided FNACs. BRAF V600E‐mutation analysis was performed using two methods, an allele‐specific polymerase chain reaction (PCR) analyzed by capillary gel electrophoresis (PCR/Qiaxcel), and a droplet digital PCR (ddPCR) assay. A total of 80 patients underwent surgery, and histology revealed 25 patients to have PTC. Of the 25 PTCs, 23 (92%) showed a BRAF V600E‐mutation. Both mutation analysis methods (PCR/Qiaxcel and ddPCR) produced concordant results. In the ultrasound‐guided group, the preoperative diagnostic sensitivity of FNAC using the Bethesda classification alone was very high and additional BRAF V600E‐mutation analysis added little to the preoperative diagnostic sensitivity. By contrast, in the palpation‐guided group, by adding BRAF V600E‐mutation analysis, eight instead of four patients were diagnosed of having PTC. This increase in the diagnostic sensitivity was statistically significant (p < 0.05). The costs per sample were as low as 62 USD (PCR/Qiaxcel and ddPCR) and 35 USD (PCR/Qiaxcel only). Ultrasound‐guided FNAC should be aimed for when dealing with thyroid nodules. However, if palpation‐guided FNAC cannot be avoided or may be required due to resource utilization, adding BRAF V600E‐mutation analysis using the methods described in this study might significantly increase the proportion of preoperatively diagnosed PTCs. The additional costs can be considered very reasonable.</description><subject>Analysis</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Biopsy, Fine-Needle</subject><subject>BRAF</subject><subject>Capillary electrophoresis</subject><subject>Cellular biology</subject><subject>Cytology</subject><subject>DNA Mutational Analysis</subject><subject>Enzymes</subject><subject>fine‐needle aspiration cytology</subject><subject>FNAC</subject><subject>Gel electrophoresis</subject><subject>Gene mutations</subject><subject>Genetic aspects</subject><subject>Humans</subject><subject>Image-Guided Biopsy</subject><subject>Iodine</subject><subject>Mutation</subject><subject>mutation analysis</subject><subject>Original</subject><subject>Palpation</subject><subject>palpation‐guided</subject><subject>Papillary thyroid carcinoma</subject><subject>Patients</subject><subject>Polymerase chain reaction</subject><subject>Polymorphism</subject><subject>Predictive Value of Tests</subject><subject>Proto-Oncogene Proteins B-raf - genetics</subject><subject>Reproducibility of Results</subject><subject>Resource utilization</subject><subject>Statistical analysis</subject><subject>Thyroid cancer</subject><subject>Thyroid Cancer, Papillary - epidemiology</subject><subject>Thyroid Cancer, Papillary - genetics</subject><subject>Thyroid Cancer, Papillary - pathology</subject><subject>Thyroid Neoplasms - enzymology</subject><subject>Thyroid Neoplasms - genetics</subject><subject>Thyroid Neoplasms - pathology</subject><subject>Tumors</subject><subject>Ultrasonic imaging</subject><subject>Ultrasonography</subject><subject>Ultrasound</subject><subject>ultrasound‐guided</subject><issn>2056-4538</issn><issn>2056-4538</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>D8T</sourceid><sourceid>DOA</sourceid><recordid>eNp1ks1u1DAQgCMEolWpxBOgSFy47DJ2bCe-IC1LC4sqgRD0ajn-Sb3K2kuctMqNKzeekSfB2S1tFwn54L_P33hGk2XPEcwRAH6t1ls8xwV6lB1joGxGaFE9frA-yk5jXAMAoghKTJ5mRwVBlJUlHGc_V151Rkajc-1k40Psncqj8dH17tr1Yx5svpXtVvYu-N8_fjWD0wnur8YuOJ37oIfW5NZ5ky69MTrtZNy6bvcgV2Mf2tCMeT3mb78szvNLBnCW0M3Q7wnpZTtGF59lT6xsozm9nU-yb-dnX5cfZhef3q-Wi4uZYsDRrIbaVIVFWDGrOS2tRbq0HAxTHJWKE6w0q2vgHApDCFgG1BS0KjkngBQtTrLV3quDXItt5zayG0WQTuwOQtcI2aUitEakOFxrinVlKLEMV2WhMbWsIiUxJcHJNdu74o3ZDvWB7Z27XOxsrRsEqgABT_ybPZ_gjdHK-L6T7cGzwxvvrkQTrkVFoag4SoJXt4IufB9M7MXGRWXaVnoThigwJQQxYMUU6-U_6DoMXSr2RFXACCN8ymC-pxqZEnbehhRXpaHNxqngjXXpfFFSSqDgJbn_gepCjJ2xd79HIKZ-FFM_itSPCX3xMNs78G_33ZfvJgUZ_ysSy4-f8ST8A3S47P4</recordid><startdate>202111</startdate><enddate>202111</enddate><creator>Gimm, Oliver</creator><creator>Ivansson, Kristin</creator><creator>Beka, Ervin</creator><creator>Rossitti, Hugo M</creator><creator>Garvin, Stina</creator><creator>Söderkvist, Peter</creator><general>John Wiley & Sons, Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IAO</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>ABXSW</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>DG8</scope><scope>ZZAVC</scope><scope>DOA</scope></search><sort><creationdate>202111</creationdate><title>Increased diagnostic sensitivity of palpation‐guided thyroid nodule fine‐needle aspiration cytology by BRAF V600E‐mutation analysis</title><author>Gimm, Oliver ; Ivansson, Kristin ; Beka, Ervin ; Rossitti, Hugo M ; Garvin, Stina ; Söderkvist, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6091-b0be83f12c6fd957ff1d7f90e6c917c942cd6bb09903e440f605e358799401c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Analysis</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Biopsy, Fine-Needle</topic><topic>BRAF</topic><topic>Capillary electrophoresis</topic><topic>Cellular biology</topic><topic>Cytology</topic><topic>DNA Mutational Analysis</topic><topic>Enzymes</topic><topic>fine‐needle aspiration cytology</topic><topic>FNAC</topic><topic>Gel electrophoresis</topic><topic>Gene mutations</topic><topic>Genetic aspects</topic><topic>Humans</topic><topic>Image-Guided Biopsy</topic><topic>Iodine</topic><topic>Mutation</topic><topic>mutation analysis</topic><topic>Original</topic><topic>Palpation</topic><topic>palpation‐guided</topic><topic>Papillary thyroid carcinoma</topic><topic>Patients</topic><topic>Polymerase chain reaction</topic><topic>Polymorphism</topic><topic>Predictive Value of Tests</topic><topic>Proto-Oncogene Proteins B-raf - genetics</topic><topic>Reproducibility of Results</topic><topic>Resource utilization</topic><topic>Statistical analysis</topic><topic>Thyroid cancer</topic><topic>Thyroid Cancer, Papillary - epidemiology</topic><topic>Thyroid Cancer, Papillary - genetics</topic><topic>Thyroid Cancer, Papillary - pathology</topic><topic>Thyroid Neoplasms - enzymology</topic><topic>Thyroid Neoplasms - genetics</topic><topic>Thyroid Neoplasms - pathology</topic><topic>Tumors</topic><topic>Ultrasonic imaging</topic><topic>Ultrasonography</topic><topic>Ultrasound</topic><topic>ultrasound‐guided</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gimm, Oliver</creatorcontrib><creatorcontrib>Ivansson, Kristin</creatorcontrib><creatorcontrib>Beka, Ervin</creatorcontrib><creatorcontrib>Rossitti, Hugo M</creatorcontrib><creatorcontrib>Garvin, Stina</creatorcontrib><creatorcontrib>Söderkvist, Peter</creatorcontrib><collection>Wiley-Blackwell Open Access Titles</collection><collection>Wiley Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SWEPUB Linköpings universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Linköpings universitet</collection><collection>SwePub Articles full text</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>The Journal of Pathology: Clinical Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gimm, Oliver</au><au>Ivansson, Kristin</au><au>Beka, Ervin</au><au>Rossitti, Hugo M</au><au>Garvin, Stina</au><au>Söderkvist, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased diagnostic sensitivity of palpation‐guided thyroid nodule fine‐needle aspiration cytology by BRAF V600E‐mutation analysis</atitle><jtitle>The Journal of Pathology: Clinical Research</jtitle><addtitle>J Pathol Clin Res</addtitle><date>2021-11</date><risdate>2021</risdate><volume>7</volume><issue>6</issue><spage>556</spage><epage>564</epage><pages>556-564</pages><issn>2056-4538</issn><eissn>2056-4538</eissn><abstract>Papillary thyroid carcinoma (PTC) is the most common type of thyroid cancer and its incidence is increasing. Preoperative diagnosis is warranted in order to avoid ‘two‐stage’ procedures that are associated with additional costs and higher radioactive iodine remnant uptake. In the setting of thyroid cancer, somatic BRAF V600E‐mutations are highly specific for PTC and can be analyzed in aspirates from fine‐needle aspiration cytology (FNAC). The ‘gold standard’ to perform FNAC is ultrasound guidance. Here, we analyze whether adding BRAF V600E‐mutation analysis could be of value in palpation‐guided FNACs. A total of 430 consecutive patients were included. Ultrasound‐guided FNACs were performed in 251 patients and 179 patients underwent palpation‐guided FNACs. BRAF V600E‐mutation analysis was performed using two methods, an allele‐specific polymerase chain reaction (PCR) analyzed by capillary gel electrophoresis (PCR/Qiaxcel), and a droplet digital PCR (ddPCR) assay. A total of 80 patients underwent surgery, and histology revealed 25 patients to have PTC. Of the 25 PTCs, 23 (92%) showed a BRAF V600E‐mutation. Both mutation analysis methods (PCR/Qiaxcel and ddPCR) produced concordant results. In the ultrasound‐guided group, the preoperative diagnostic sensitivity of FNAC using the Bethesda classification alone was very high and additional BRAF V600E‐mutation analysis added little to the preoperative diagnostic sensitivity. By contrast, in the palpation‐guided group, by adding BRAF V600E‐mutation analysis, eight instead of four patients were diagnosed of having PTC. This increase in the diagnostic sensitivity was statistically significant (p < 0.05). The costs per sample were as low as 62 USD (PCR/Qiaxcel and ddPCR) and 35 USD (PCR/Qiaxcel only). Ultrasound‐guided FNAC should be aimed for when dealing with thyroid nodules. However, if palpation‐guided FNAC cannot be avoided or may be required due to resource utilization, adding BRAF V600E‐mutation analysis using the methods described in this study might significantly increase the proportion of preoperatively diagnosed PTCs. The additional costs can be considered very reasonable.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>34156770</pmid><doi>10.1002/cjp2.231</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Biomarkers, Tumor - genetics Biopsy, Fine-Needle BRAF Capillary electrophoresis Cellular biology Cytology DNA Mutational Analysis Enzymes fine‐needle aspiration cytology FNAC Gel electrophoresis Gene mutations Genetic aspects Humans Image-Guided Biopsy Iodine Mutation mutation analysis Original Palpation palpation‐guided Papillary thyroid carcinoma Patients Polymerase chain reaction Polymorphism Predictive Value of Tests Proto-Oncogene Proteins B-raf - genetics Reproducibility of Results Resource utilization Statistical analysis Thyroid cancer Thyroid Cancer, Papillary - epidemiology Thyroid Cancer, Papillary - genetics Thyroid Cancer, Papillary - pathology Thyroid Neoplasms - enzymology Thyroid Neoplasms - genetics Thyroid Neoplasms - pathology Tumors Ultrasonic imaging Ultrasonography Ultrasound ultrasound‐guided |
title | Increased diagnostic sensitivity of palpation‐guided thyroid nodule fine‐needle aspiration cytology by BRAF V600E‐mutation analysis |
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