Chromophobe renal cell carcinoma with sarcomatoid and heterologous osteosarcoma-like differentiation: a case report and literature review
Abstract Chromophobe renal cell carcinoma (CRCC) is a subtype of renal cell carcinoma (RCC) with a favorable prognosis. Sarcomatoid differentiation in RCC is assumed to be the outcome of the parent tumor’s dedifferentiation and associated with poorer prognosis. Sarcomatoid differentiation can be det...
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Veröffentlicht in: | Journal of surgical case reports 2023-08, Vol.2023 (8) |
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container_title | Journal of surgical case reports |
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creator | Abuorouq, Saleh Sahawneh, Firas Halalsheh, Omar Haddad, Husam K Mekail, Raed Alzoubi, Hiba Alrjoub, Mo’ath Serhan, Hashem A |
description | Abstract
Chromophobe renal cell carcinoma (CRCC) is a subtype of renal cell carcinoma (RCC) with a favorable prognosis. Sarcomatoid differentiation in RCC is assumed to be the outcome of the parent tumor’s dedifferentiation and associated with poorer prognosis. Sarcomatoid differentiation can be detected in CRCC as well as other subtypes, but the occurrence of divergent osteosarcoma-like components in sarcomatoid CRCC is extremely unusual. Only six cases have been previously reported in the literature, we reviewed them and presented the seventh case in a 71-year-old male who had a left kidney heterogeneous mass. The resected tumor showed a sarcoma-like spindle cell area with an adjacent osteosarcoma area producing lacy bone material and bony trabeculae in a hard area mixed with a typical CRCC. In conclusion, sarcomatoid CRCC with osteosarcomatous differentiation is a very rare tumor and should be kept in mind especially when dealing with small or frozen sections biopsies. |
doi_str_mv | 10.1093/jscr/rjad476 |
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Chromophobe renal cell carcinoma (CRCC) is a subtype of renal cell carcinoma (RCC) with a favorable prognosis. Sarcomatoid differentiation in RCC is assumed to be the outcome of the parent tumor’s dedifferentiation and associated with poorer prognosis. Sarcomatoid differentiation can be detected in CRCC as well as other subtypes, but the occurrence of divergent osteosarcoma-like components in sarcomatoid CRCC is extremely unusual. Only six cases have been previously reported in the literature, we reviewed them and presented the seventh case in a 71-year-old male who had a left kidney heterogeneous mass. The resected tumor showed a sarcoma-like spindle cell area with an adjacent osteosarcoma area producing lacy bone material and bony trabeculae in a hard area mixed with a typical CRCC. In conclusion, sarcomatoid CRCC with osteosarcomatous differentiation is a very rare tumor and should be kept in mind especially when dealing with small or frozen sections biopsies.</description><identifier>ISSN: 2042-8812</identifier><identifier>EISSN: 2042-8812</identifier><identifier>DOI: 10.1093/jscr/rjad476</identifier><language>eng</language><publisher>Oxford University Press</publisher><subject>Case Series</subject><ispartof>Journal of surgical case reports, 2023-08, Vol.2023 (8)</ispartof><rights>Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2023. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c318t-16f0a1f71695cc31966d780b90c6070d451b9d919bb8c7da00f7fa546729ea2d3</cites><orcidid>0000-0002-2953-2188</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10447077/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10447077/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,1598,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Abuorouq, Saleh</creatorcontrib><creatorcontrib>Sahawneh, Firas</creatorcontrib><creatorcontrib>Halalsheh, Omar</creatorcontrib><creatorcontrib>Haddad, Husam K</creatorcontrib><creatorcontrib>Mekail, Raed</creatorcontrib><creatorcontrib>Alzoubi, Hiba</creatorcontrib><creatorcontrib>Alrjoub, Mo’ath</creatorcontrib><creatorcontrib>Serhan, Hashem A</creatorcontrib><title>Chromophobe renal cell carcinoma with sarcomatoid and heterologous osteosarcoma-like differentiation: a case report and literature review</title><title>Journal of surgical case reports</title><description>Abstract
Chromophobe renal cell carcinoma (CRCC) is a subtype of renal cell carcinoma (RCC) with a favorable prognosis. Sarcomatoid differentiation in RCC is assumed to be the outcome of the parent tumor’s dedifferentiation and associated with poorer prognosis. Sarcomatoid differentiation can be detected in CRCC as well as other subtypes, but the occurrence of divergent osteosarcoma-like components in sarcomatoid CRCC is extremely unusual. Only six cases have been previously reported in the literature, we reviewed them and presented the seventh case in a 71-year-old male who had a left kidney heterogeneous mass. The resected tumor showed a sarcoma-like spindle cell area with an adjacent osteosarcoma area producing lacy bone material and bony trabeculae in a hard area mixed with a typical CRCC. In conclusion, sarcomatoid CRCC with osteosarcomatous differentiation is a very rare tumor and should be kept in mind especially when dealing with small or frozen sections biopsies.</description><subject>Case Series</subject><issn>2042-8812</issn><issn>2042-8812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNp9kbtOwzAUhi0EEhV04wG8sRBqp6kdsyBUcZMqscBsOb40Lkkc2U4rHoG3xqEVgoUz-Fz8n8-WfgAuMLrGiM1nmyD9zG-EKig5ApMcFXlWljg__lWfgmkIG5SiYBiXZAI-l7V3retrV2nodScaKHWTDuGl7Vwr4M7GGobUpiY6q6DoFKx11N41bu2GAF2I2h0UWWPfNVTWGJ1o0YpoXXcDRQKG8YHe-fhNaGwiiDj4cbq1encOToxogp4e8hl4e7h_XT5lq5fH5-XdKpNzXMYME4MENhQTtpBpxAhRtEQVQ5IgilSxwBVTDLOqKiVVAiFDjVgUhOZMi1zNz8DtntsPVauVTL_0ouG9t63wH9wJy__edLbma7flGBUFRZQmwtWeIL0LwWvzs4wRH73goxf84EWSX-7lbuj_V34BxuiRPg</recordid><startdate>20230804</startdate><enddate>20230804</enddate><creator>Abuorouq, Saleh</creator><creator>Sahawneh, Firas</creator><creator>Halalsheh, Omar</creator><creator>Haddad, Husam K</creator><creator>Mekail, Raed</creator><creator>Alzoubi, Hiba</creator><creator>Alrjoub, Mo’ath</creator><creator>Serhan, Hashem A</creator><general>Oxford University Press</general><scope>TOX</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2953-2188</orcidid></search><sort><creationdate>20230804</creationdate><title>Chromophobe renal cell carcinoma with sarcomatoid and heterologous osteosarcoma-like differentiation: a case report and literature review</title><author>Abuorouq, Saleh ; Sahawneh, Firas ; Halalsheh, Omar ; Haddad, Husam K ; Mekail, Raed ; Alzoubi, Hiba ; Alrjoub, Mo’ath ; Serhan, Hashem A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c318t-16f0a1f71695cc31966d780b90c6070d451b9d919bb8c7da00f7fa546729ea2d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Case Series</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abuorouq, Saleh</creatorcontrib><creatorcontrib>Sahawneh, Firas</creatorcontrib><creatorcontrib>Halalsheh, Omar</creatorcontrib><creatorcontrib>Haddad, Husam K</creatorcontrib><creatorcontrib>Mekail, Raed</creatorcontrib><creatorcontrib>Alzoubi, Hiba</creatorcontrib><creatorcontrib>Alrjoub, Mo’ath</creatorcontrib><creatorcontrib>Serhan, Hashem A</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of surgical case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abuorouq, Saleh</au><au>Sahawneh, Firas</au><au>Halalsheh, Omar</au><au>Haddad, Husam K</au><au>Mekail, Raed</au><au>Alzoubi, Hiba</au><au>Alrjoub, Mo’ath</au><au>Serhan, Hashem A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chromophobe renal cell carcinoma with sarcomatoid and heterologous osteosarcoma-like differentiation: a case report and literature review</atitle><jtitle>Journal of surgical case reports</jtitle><date>2023-08-04</date><risdate>2023</risdate><volume>2023</volume><issue>8</issue><issn>2042-8812</issn><eissn>2042-8812</eissn><abstract>Abstract
Chromophobe renal cell carcinoma (CRCC) is a subtype of renal cell carcinoma (RCC) with a favorable prognosis. Sarcomatoid differentiation in RCC is assumed to be the outcome of the parent tumor’s dedifferentiation and associated with poorer prognosis. Sarcomatoid differentiation can be detected in CRCC as well as other subtypes, but the occurrence of divergent osteosarcoma-like components in sarcomatoid CRCC is extremely unusual. Only six cases have been previously reported in the literature, we reviewed them and presented the seventh case in a 71-year-old male who had a left kidney heterogeneous mass. The resected tumor showed a sarcoma-like spindle cell area with an adjacent osteosarcoma area producing lacy bone material and bony trabeculae in a hard area mixed with a typical CRCC. In conclusion, sarcomatoid CRCC with osteosarcomatous differentiation is a very rare tumor and should be kept in mind especially when dealing with small or frozen sections biopsies.</abstract><pub>Oxford University Press</pub><doi>10.1093/jscr/rjad476</doi><orcidid>https://orcid.org/0000-0002-2953-2188</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Case Series |
title | Chromophobe renal cell carcinoma with sarcomatoid and heterologous osteosarcoma-like differentiation: a case report and literature review |
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