CIC‐associated round cell sarcoma of the small bowel
Small round cell sarcoma (SRCS) is considered a highly aggressive soft tissue tumour. The World Health Organization (WHO) has recognized a distinct subtype in view of the recently discovered CIC fusion gene. It has shown to have distinct pathophysiology and prognosis unlike Ewing sarcoma (ES) and rh...
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Veröffentlicht in: | Surgical practice 2020-02, Vol.24 (1), p.40-42 |
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description | Small round cell sarcoma (SRCS) is considered a highly aggressive soft tissue tumour. The World Health Organization (WHO) has recognized a distinct subtype in view of the recently discovered CIC fusion gene. It has shown to have distinct pathophysiology and prognosis unlike Ewing sarcoma (ES) and rhabdomyosarcoma. However, due to its rarity, no standardized treatment has been concluded. We reported a case of intestinal obstruction caused by small bowel associated associated, laparotomy and small bowel resection was performed with good recovery and 1 year free disease survival. The gold standard of diagnosis with molecular confirmation is utmostly important in order to learn more about the natural history of this subtype thus formulating the best management plan. |
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The World Health Organization (WHO) has recognized a distinct subtype in view of the recently discovered CIC fusion gene. It has shown to have distinct pathophysiology and prognosis unlike Ewing sarcoma (ES) and rhabdomyosarcoma. However, due to its rarity, no standardized treatment has been concluded. We reported a case of intestinal obstruction caused by small bowel associated associated, laparotomy and small bowel resection was performed with good recovery and 1 year free disease survival. The gold standard of diagnosis with molecular confirmation is utmostly important in order to learn more about the natural history of this subtype thus formulating the best management plan.</description><identifier>ISSN: 1744-1625</identifier><identifier>EISSN: 1744-1633</identifier><identifier>DOI: 10.1111/1744-1633.12411</identifier><language>eng</language><publisher>Melbourne: Wiley Publishing Asia Pty Ltd</publisher><subject>Medical prognosis ; Sarcoma ; Small intestine</subject><ispartof>Surgical practice, 2020-02, Vol.24 (1), p.40-42</ispartof><rights>2019 College of Surgeons of Hong Kong</rights><rights>2020 College of Surgeons of Hong Kong</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2691-3bf738911160eebe0882c39b0ff10a8dace6fa6bdb4d7aeae941d105534108643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1744-1633.12411$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1744-1633.12411$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Chan, Angus C.K.</creatorcontrib><creatorcontrib>Chiu, Jennifer H.F.</creatorcontrib><creatorcontrib>Lau, Kevin C.N.</creatorcontrib><title>CIC‐associated round cell sarcoma of the small bowel</title><title>Surgical practice</title><description>Small round cell sarcoma (SRCS) is considered a highly aggressive soft tissue tumour. The World Health Organization (WHO) has recognized a distinct subtype in view of the recently discovered CIC fusion gene. It has shown to have distinct pathophysiology and prognosis unlike Ewing sarcoma (ES) and rhabdomyosarcoma. However, due to its rarity, no standardized treatment has been concluded. We reported a case of intestinal obstruction caused by small bowel associated associated, laparotomy and small bowel resection was performed with good recovery and 1 year free disease survival. The gold standard of diagnosis with molecular confirmation is utmostly important in order to learn more about the natural history of this subtype thus formulating the best management plan.</description><subject>Medical prognosis</subject><subject>Sarcoma</subject><subject>Small intestine</subject><issn>1744-1625</issn><issn>1744-1633</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFULFOwzAQtRBIlMLMGok5rS92HGesIqCVKjEAs-U4Z5EqqYudqurGJ_CNfEkTgrpyy52e3rt39wi5BzqDvuaQcR6DYGwGCQe4IJMzcnmek_Sa3ISwoZRlMmMTIopV8fP1rUNwptYdVpF3-20VGWyaKGhvXKsjZ6PuA6PQ6h4s3QGbW3JldRPw7q9PyfvT41uxjNcvz6tisY5NInKIWWkzJvP-PEERS6RSJoblJbUWqJaVNiisFmVV8irTqDHnUAFNU8aBSsHZlDyMe3fefe4xdGrj9n7bW6qEpTmXNKV5z5qPLONdCB6t2vm61f6ogKohHDW8r4Yo1G84vSIdFYe6weN_dLV4XY66E4AbZTU</recordid><startdate>202002</startdate><enddate>202002</enddate><creator>Chan, Angus C.K.</creator><creator>Chiu, Jennifer H.F.</creator><creator>Lau, Kevin C.N.</creator><general>Wiley Publishing Asia Pty Ltd</general><general>Blackwell Publishing Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope></search><sort><creationdate>202002</creationdate><title>CIC‐associated round cell sarcoma of the small bowel</title><author>Chan, Angus C.K. ; Chiu, Jennifer H.F. ; Lau, Kevin C.N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2691-3bf738911160eebe0882c39b0ff10a8dace6fa6bdb4d7aeae941d105534108643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Medical prognosis</topic><topic>Sarcoma</topic><topic>Small intestine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chan, Angus C.K.</creatorcontrib><creatorcontrib>Chiu, Jennifer H.F.</creatorcontrib><creatorcontrib>Lau, Kevin C.N.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Surgical practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chan, Angus C.K.</au><au>Chiu, Jennifer H.F.</au><au>Lau, Kevin C.N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CIC‐associated round cell sarcoma of the small bowel</atitle><jtitle>Surgical practice</jtitle><date>2020-02</date><risdate>2020</risdate><volume>24</volume><issue>1</issue><spage>40</spage><epage>42</epage><pages>40-42</pages><issn>1744-1625</issn><eissn>1744-1633</eissn><abstract>Small round cell sarcoma (SRCS) is considered a highly aggressive soft tissue tumour. The World Health Organization (WHO) has recognized a distinct subtype in view of the recently discovered CIC fusion gene. It has shown to have distinct pathophysiology and prognosis unlike Ewing sarcoma (ES) and rhabdomyosarcoma. However, due to its rarity, no standardized treatment has been concluded. We reported a case of intestinal obstruction caused by small bowel associated associated, laparotomy and small bowel resection was performed with good recovery and 1 year free disease survival. The gold standard of diagnosis with molecular confirmation is utmostly important in order to learn more about the natural history of this subtype thus formulating the best management plan.</abstract><cop>Melbourne</cop><pub>Wiley Publishing Asia Pty Ltd</pub><doi>10.1111/1744-1633.12411</doi><tpages>3</tpages></addata></record> |
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subjects | Medical prognosis Sarcoma Small intestine |
title | CIC‐associated round cell sarcoma of the small bowel |
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