A subset of prostatic basal cell carcinomas harbor the MYB rearrangement of adenoid cystic carcinoma

Summary Adenoid cystic carcinoma (ACC) is a basaloid tumor consisting of myoepithelial and ductal cells typically arranged in a cribriform pattern. Adenoid cystic carcinoma is generally regarded as a form of salivary gland carcinoma, but it can arise from sites unassociated with salivary tissue. A r...

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Veröffentlicht in:Human pathology 2015-08, Vol.46 (8), p.1204-1208
Hauptverfasser: Bishop, Justin A., MD, Yonescu, Raluca, MD, Epstein, Jonathan I., MD, Westra, William H., MD
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container_end_page 1208
container_issue 8
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container_title Human pathology
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creator Bishop, Justin A., MD
Yonescu, Raluca, MD
Epstein, Jonathan I., MD
Westra, William H., MD
description Summary Adenoid cystic carcinoma (ACC) is a basaloid tumor consisting of myoepithelial and ductal cells typically arranged in a cribriform pattern. Adenoid cystic carcinoma is generally regarded as a form of salivary gland carcinoma, but it can arise from sites unassociated with salivary tissue. A rare form of prostate carcinoma exhibits ACC-like features; it is no longer regarded as a true ACC but rather as prostatic basal cell carcinoma (PBCC) and within the spectrum of basaloid prostatic proliferations. True ACCs often harbor MYB translocations resulting in the MYB-NFIB fusion protein. MYB analysis could clarify the true nature of prostatic carcinomas that exhibit ACC features and thus help refine the classification of prostatic basaloid proliferations. Twelve PBCCs were identified from the pathology consultation files of Johns Hopkins Hospital. The histopathologic features were reviewed, and break-apart fluorescence in situ hybridization for MYB was performed. All 12 cases exhibited prominent basaloid histology. Four were purely solid, 7 exhibited a cribriform pattern reminiscent of salivary ACC, and 1 had a mixed pattern. The MYB rearrangement was detected in 2 (29%) of 7 ACC-like carcinomas but in none (0%) of the 5 PBCCs with a prominent solid pattern. True ACCs can arise in the prostate as is evidenced by the presence of the characteristic MYB rearrangement. When dealing with malignant basaloid proliferations in the prostate, recommendations to consolidate ACCs with other tumor types may need to be reassessed, particularly in light of the rapidly advancing field of biologic therapy where the identification of tumor-specific genetic alterations presents novel therapeutic targets.
doi_str_mv 10.1016/j.humpath.2015.05.002
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Adenoid cystic carcinoma is generally regarded as a form of salivary gland carcinoma, but it can arise from sites unassociated with salivary tissue. A rare form of prostate carcinoma exhibits ACC-like features; it is no longer regarded as a true ACC but rather as prostatic basal cell carcinoma (PBCC) and within the spectrum of basaloid prostatic proliferations. True ACCs often harbor MYB translocations resulting in the MYB-NFIB fusion protein. MYB analysis could clarify the true nature of prostatic carcinomas that exhibit ACC features and thus help refine the classification of prostatic basaloid proliferations. Twelve PBCCs were identified from the pathology consultation files of Johns Hopkins Hospital. The histopathologic features were reviewed, and break-apart fluorescence in situ hybridization for MYB was performed. All 12 cases exhibited prominent basaloid histology. Four were purely solid, 7 exhibited a cribriform pattern reminiscent of salivary ACC, and 1 had a mixed pattern. The MYB rearrangement was detected in 2 (29%) of 7 ACC-like carcinomas but in none (0%) of the 5 PBCCs with a prominent solid pattern. True ACCs can arise in the prostate as is evidenced by the presence of the characteristic MYB rearrangement. When dealing with malignant basaloid proliferations in the prostate, recommendations to consolidate ACCs with other tumor types may need to be reassessed, particularly in light of the rapidly advancing field of biologic therapy where the identification of tumor-specific genetic alterations presents novel therapeutic targets.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1016/j.humpath.2015.05.002</identifier><identifier>PMID: 26089205</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adenoid cystic carcinoma ; Aged ; Aged, 80 and over ; Basal cell carcinoma ; Carcinoma, Adenoid Cystic - genetics ; Carcinoma, Adenoid Cystic - pathology ; Carcinoma, Basal Cell - genetics ; Carcinoma, Basal Cell - pathology ; Classification ; Classification schemes ; Fluorescence in situ hybridization ; Gangrene ; Genes ; Genes, myb - genetics ; Humans ; Hybridization ; In Situ Hybridization, Fluorescence ; Male ; Morphology ; MYB-NFIB ; Oncogene Proteins, Fusion - genetics ; Pathology ; Prostate ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - pathology ; Studies ; Sunscreen ; Transcription factors ; Tumors</subject><ispartof>Human pathology, 2015-08, Vol.46 (8), p.1204-1208</ispartof><rights>Elsevier Inc.</rights><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. 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Adenoid cystic carcinoma is generally regarded as a form of salivary gland carcinoma, but it can arise from sites unassociated with salivary tissue. A rare form of prostate carcinoma exhibits ACC-like features; it is no longer regarded as a true ACC but rather as prostatic basal cell carcinoma (PBCC) and within the spectrum of basaloid prostatic proliferations. True ACCs often harbor MYB translocations resulting in the MYB-NFIB fusion protein. MYB analysis could clarify the true nature of prostatic carcinomas that exhibit ACC features and thus help refine the classification of prostatic basaloid proliferations. Twelve PBCCs were identified from the pathology consultation files of Johns Hopkins Hospital. The histopathologic features were reviewed, and break-apart fluorescence in situ hybridization for MYB was performed. All 12 cases exhibited prominent basaloid histology. Four were purely solid, 7 exhibited a cribriform pattern reminiscent of salivary ACC, and 1 had a mixed pattern. The MYB rearrangement was detected in 2 (29%) of 7 ACC-like carcinomas but in none (0%) of the 5 PBCCs with a prominent solid pattern. True ACCs can arise in the prostate as is evidenced by the presence of the characteristic MYB rearrangement. When dealing with malignant basaloid proliferations in the prostate, recommendations to consolidate ACCs with other tumor types may need to be reassessed, particularly in light of the rapidly advancing field of biologic therapy where the identification of tumor-specific genetic alterations presents novel therapeutic targets.</description><subject>Adenoid cystic carcinoma</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Basal cell carcinoma</subject><subject>Carcinoma, Adenoid Cystic - genetics</subject><subject>Carcinoma, Adenoid Cystic - pathology</subject><subject>Carcinoma, Basal Cell - genetics</subject><subject>Carcinoma, Basal Cell - pathology</subject><subject>Classification</subject><subject>Classification schemes</subject><subject>Fluorescence in situ hybridization</subject><subject>Gangrene</subject><subject>Genes</subject><subject>Genes, myb - genetics</subject><subject>Humans</subject><subject>Hybridization</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Male</subject><subject>Morphology</subject><subject>MYB-NFIB</subject><subject>Oncogene Proteins, Fusion - genetics</subject><subject>Pathology</subject><subject>Prostate</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Studies</subject><subject>Sunscreen</subject><subject>Transcription factors</subject><subject>Tumors</subject><issn>0046-8177</issn><issn>1532-8392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUk1v1DAQtRAV3RZ-AsgSFy7ZepzYSS6gUhWoVMQBOHCyJvaE9ZKPrZ0g7b_HYZdW6gVpNL689zzvzTD2EsQaBOiL7Xoz9zucNmspQK1FKiGfsBWoXGZVXsunbCVEobMKyvKUncW4FQJAFeoZO5VaVLUUasXcJY9zE2niY8t3YYwTTt7yBiN23FKXGgbrh7HHyDcYmjHwaUP884_3PBCGgMNP6mn4y0dHw-gdt_u4iNwzn7OTFrtIL47vOfv-4frb1afs9svHm6vL28yqqpiyRrkCIQcqUQFqVHmj2lIVUljSqm5LLMFaVxeuzVslRUVOIpWywULWJGV-zt4cdJORu5niZHofFxM40DhHA7quaqU1QIK-fgTdjnMY0nQGSlFBkeR0QqkDyqZkYqDW7ILvMewNCLOswWzNcQ1mWYMRqcQyyKuj-tz05O5Z_3JPgHcHAKU4fnsKJlpPgyXnA9nJuNH_94u3jxRs5wdvsftFe4oPbkyURpivyy0spwAqnYGqq_wPDlKwYQ</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Bishop, Justin A., MD</creator><creator>Yonescu, Raluca, MD</creator><creator>Epstein, Jonathan I., MD</creator><creator>Westra, William H., MD</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><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>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9743-4360</orcidid></search><sort><creationdate>20150801</creationdate><title>A subset of prostatic basal cell carcinomas harbor the MYB rearrangement of adenoid cystic carcinoma</title><author>Bishop, Justin A., MD ; Yonescu, Raluca, MD ; Epstein, Jonathan I., MD ; Westra, William H., MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c584t-b5d4a131e7a51a6a53b5f75420ce659f7a71ccd94df3f5208ed2ae72ba429e223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adenoid cystic carcinoma</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Basal cell carcinoma</topic><topic>Carcinoma, Adenoid Cystic - genetics</topic><topic>Carcinoma, Adenoid Cystic - pathology</topic><topic>Carcinoma, Basal Cell - genetics</topic><topic>Carcinoma, Basal Cell - pathology</topic><topic>Classification</topic><topic>Classification schemes</topic><topic>Fluorescence in situ hybridization</topic><topic>Gangrene</topic><topic>Genes</topic><topic>Genes, myb - genetics</topic><topic>Humans</topic><topic>Hybridization</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Male</topic><topic>Morphology</topic><topic>MYB-NFIB</topic><topic>Oncogene Proteins, Fusion - genetics</topic><topic>Pathology</topic><topic>Prostate</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Studies</topic><topic>Sunscreen</topic><topic>Transcription factors</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bishop, Justin A., MD</creatorcontrib><creatorcontrib>Yonescu, Raluca, MD</creatorcontrib><creatorcontrib>Epstein, Jonathan I., MD</creatorcontrib><creatorcontrib>Westra, William H., MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; 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Adenoid cystic carcinoma is generally regarded as a form of salivary gland carcinoma, but it can arise from sites unassociated with salivary tissue. A rare form of prostate carcinoma exhibits ACC-like features; it is no longer regarded as a true ACC but rather as prostatic basal cell carcinoma (PBCC) and within the spectrum of basaloid prostatic proliferations. True ACCs often harbor MYB translocations resulting in the MYB-NFIB fusion protein. MYB analysis could clarify the true nature of prostatic carcinomas that exhibit ACC features and thus help refine the classification of prostatic basaloid proliferations. Twelve PBCCs were identified from the pathology consultation files of Johns Hopkins Hospital. The histopathologic features were reviewed, and break-apart fluorescence in situ hybridization for MYB was performed. All 12 cases exhibited prominent basaloid histology. Four were purely solid, 7 exhibited a cribriform pattern reminiscent of salivary ACC, and 1 had a mixed pattern. The MYB rearrangement was detected in 2 (29%) of 7 ACC-like carcinomas but in none (0%) of the 5 PBCCs with a prominent solid pattern. True ACCs can arise in the prostate as is evidenced by the presence of the characteristic MYB rearrangement. When dealing with malignant basaloid proliferations in the prostate, recommendations to consolidate ACCs with other tumor types may need to be reassessed, particularly in light of the rapidly advancing field of biologic therapy where the identification of tumor-specific genetic alterations presents novel therapeutic targets.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26089205</pmid><doi>10.1016/j.humpath.2015.05.002</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-9743-4360</orcidid></addata></record>
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subjects Adenoid cystic carcinoma
Aged
Aged, 80 and over
Basal cell carcinoma
Carcinoma, Adenoid Cystic - genetics
Carcinoma, Adenoid Cystic - pathology
Carcinoma, Basal Cell - genetics
Carcinoma, Basal Cell - pathology
Classification
Classification schemes
Fluorescence in situ hybridization
Gangrene
Genes
Genes, myb - genetics
Humans
Hybridization
In Situ Hybridization, Fluorescence
Male
Morphology
MYB-NFIB
Oncogene Proteins, Fusion - genetics
Pathology
Prostate
Prostatic Neoplasms - genetics
Prostatic Neoplasms - pathology
Studies
Sunscreen
Transcription factors
Tumors
title A subset of prostatic basal cell carcinomas harbor the MYB rearrangement of adenoid cystic carcinoma
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