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NR4A3 Immunostain Is a Highly Sensitive and Specific Marker for Acinic Cell Carcinoma in Cytologic and Surgical Specimens

dc.contributor.authorViswanathan, K
dc.contributor.authorBeg, S
dc.contributor.authorHe, B
dc.contributor.authorZhang, T
dc.contributor.authorCantley, R
dc.contributor.authorLubin, DJ
dc.contributor.authorShi, Q
dc.contributor.authorMaleki, Z
dc.contributor.authorAsiry, S
dc.contributor.authorRao, R
dc.contributor.authorKatabi, N
dc.contributor.authorNakaguro, M
dc.contributor.authorFaquin, WC
dc.contributor.authorSadow, PM
dc.contributor.authorSiddiqui, MT
dc.contributor.authorScognamiglio, T
dc.coverage.spatialEngland
dc.date.accessioned2023-04-27T16:04:26Z
dc.date.available2023-04-27T16:04:26Z
dc.date.issued2022-01-01
dc.identifier.issn0002-9173
dc.identifier.issn1943-7722
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pubmed/34508546
dc.identifier.urihttps://hdl.handle.net/2027.42/176224en
dc.description.abstractObjectives: Salivary gland acinic cell carcinoma (AciCC) has recognizable cytomorphologic features that can overlap with benign and malignant entities, creating a diagnostic challenge. AciCC harbors a t(4;9) translocation increasing nuclear receptor subfamily 4 group A member 3 (NR4A3) expression, detectable by immunohistochemistry (IHC) on surgical resection (SR). NR4A3 IHC cytology data are limited. Here, we examine NR4A3 IHC on smears, cell blocks (CBs), and SRs of AciCC and its mimickers. Methods: Our cohort comprised AciCC (including high-grade transformation), secretory carcinoma, mucoepidermoid carcinoma (MEC), Warthin tumor, pleomorphic adenoma (PA), cellular PA, carcinoma ex-PA, oncocytic carcinoma, oncocytoma, and nodular oncocytosis. NR4A3 IHC (Santa Cruz Biotechnology and Origene antibodies) was positive if more than 5% tumor cells showed nuclear staining. Results: Among CBs, 90% of AciCC cases and none of the mimickers expressed NR4A3. Among SRs, 100% of AciCC cases showed diffuse NR4A3, whereas one high-grade MEC expressed focal NR4A3. Concordance was 95% with two antibody clones. Sensitivity, specificity, positive predictive value, and negative predictive value were 90%, 100%, 100%, and 94.7% for CBs and 100%, 98.8%, 92.3%, and 100% for SRs, respectively. NR4A3 immunostaining was demonstrable on smears from an AciCC case. Conclusions: NR4A3 IHC can be a robust diagnostic tool to identify AciCC, especially for cytology specimens.
dc.format.mediumPrint
dc.languageeng
dc.publisherOxford University Press (OUP)
dc.subjectAcinic cell carcinoma
dc.subjectNR4A3
dc.subjectOncocytic
dc.subjectSalivary
dc.subjectBiomarkers, Tumor
dc.subjectCarcinoma, Acinar Cell
dc.subjectCarcinoma, Mucoepidermoid
dc.subjectDNA-Binding Proteins
dc.subjectHumans
dc.subjectImmunohistochemistry
dc.subjectReceptors, Steroid
dc.subjectReceptors, Thyroid Hormone
dc.subjectSalivary Gland Neoplasms
dc.titleNR4A3 Immunostain Is a Highly Sensitive and Specific Marker for Acinic Cell Carcinoma in Cytologic and Surgical Specimens
dc.typeArticle
dc.identifier.pmid34508546
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/176224/2/aqab099.pdf
dc.identifier.doi10.1093/ajcp/aqab099
dc.identifier.doihttps://dx.doi.org/10.7302/7163
dc.identifier.sourceAmerican Journal of Clinical Pathology
dc.description.versionPublished version
dc.date.updated2023-04-27T16:04:20Z
dc.identifier.orcid0000-0003-0031-0001
dc.identifier.orcid0000-0002-0409-2374
dc.identifier.orcid0000-0003-3273-4802
dc.identifier.orcid0000-0002-5776-8366
dc.identifier.volume157
dc.identifier.issue1
dc.identifier.startpage98
dc.identifier.endpage108
dc.identifier.name-orcidViswanathan, K; 0000-0003-0031-0001
dc.identifier.name-orcidBeg, S
dc.identifier.name-orcidHe, B
dc.identifier.name-orcidZhang, T
dc.identifier.name-orcidCantley, R
dc.identifier.name-orcidLubin, DJ; 0000-0002-0409-2374
dc.identifier.name-orcidShi, Q
dc.identifier.name-orcidMaleki, Z; 0000-0003-3273-4802
dc.identifier.name-orcidAsiry, S
dc.identifier.name-orcidRao, R; 0000-0002-5776-8366
dc.identifier.name-orcidKatabi, N
dc.identifier.name-orcidNakaguro, M
dc.identifier.name-orcidFaquin, WC
dc.identifier.name-orcidSadow, PM
dc.identifier.name-orcidSiddiqui, MT
dc.identifier.name-orcidScognamiglio, T
dc.working.doi10.7302/7163en
dc.owningcollnamePathology, Department of


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