Diagnosis, treatment, radiologic and pathologic findings of splenic angiosarcoma; a case report
Primer splenik anjiosarkomalar dalağın hematopoetik sistemle ilişkili olmayan en sık malign tümörleri(1) olmasına karşın oldukça nadir görülmekte ve prognozu son derece kötüdür(2). Bu tümörlerin seyri oldukça agresif ve ölümcül olup yaygın metastazlar veya dalak rüptürü ile karşımıza çıkarlar(1). Ke...
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Veröffentlicht in: | Marmara Medical Journal 2009, Vol.22 (1), p.56-58 |
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creator | YALMAN, Haydar YİĞİTBAŞI, Rafet DEMİRAL, Gökhan OKUR, Özlem EVCİMİK, Taner EKİNCİ, Özgür AKSOY, Fikret |
description | Primer splenik anjiosarkomalar dalağın hematopoetik sistemle ilişkili olmayan en sık malign tümörleri(1) olmasına karşın oldukça nadir görülmekte ve prognozu son derece kötüdür(2). Bu tümörlerin seyri oldukça agresif ve ölümcül olup yaygın metastazlar veya dalak rüptürü ile karşımıza çıkarlar(1). Kesin tanı ve tedavi cerrahi ile olur ve rüptür öncesi uygulanan splenektomi yaşam süresini anlamlı şekilde uzatır(5). Primer splenik anjiosarkomalı bir hastanın tanı, radyolojik patolojik bulgular ve tedavisini sunuyoruz.
Although primary splenic angiosarcomas are the most common malignant nonhematopoietic tumors of spleen(1) ,they are extremely rare tumors with very poor prognosis(2). These tumors are highly aggressive and lethal,present with widespread metastasis or splenic rupture(1). Definitive diagnosis and treatment is surgical and survival is significantly improved when splenectomy is performed prior to rupture(5). Diagnosis, radiologic and pathologic findings and treatment of a patient with primary splenic angiosarcoma is presented. |
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Although primary splenic angiosarcomas are the most common malignant nonhematopoietic tumors of spleen(1) ,they are extremely rare tumors with very poor prognosis(2). These tumors are highly aggressive and lethal,present with widespread metastasis or splenic rupture(1). Definitive diagnosis and treatment is surgical and survival is significantly improved when splenectomy is performed prior to rupture(5). Diagnosis, radiologic and pathologic findings and treatment of a patient with primary splenic angiosarcoma is presented.</description><identifier>ISSN: 1019-1941</identifier><language>eng</language><publisher>Marmara Üniversitesi</publisher><ispartof>Marmara Medical Journal, 2009, Vol.22 (1), p.56-58</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,4010</link.rule.ids></links><search><creatorcontrib>YALMAN, Haydar</creatorcontrib><creatorcontrib>YİĞİTBAŞI, Rafet</creatorcontrib><creatorcontrib>DEMİRAL, Gökhan</creatorcontrib><creatorcontrib>OKUR, Özlem</creatorcontrib><creatorcontrib>EVCİMİK, Taner</creatorcontrib><creatorcontrib>EKİNCİ, Özgür</creatorcontrib><creatorcontrib>AKSOY, Fikret</creatorcontrib><title>Diagnosis, treatment, radiologic and pathologic findings of splenic angiosarcoma; a case report</title><title>Marmara Medical Journal</title><description>Primer splenik anjiosarkomalar dalağın hematopoetik sistemle ilişkili olmayan en sık malign tümörleri(1) olmasına karşın oldukça nadir görülmekte ve prognozu son derece kötüdür(2). Bu tümörlerin seyri oldukça agresif ve ölümcül olup yaygın metastazlar veya dalak rüptürü ile karşımıza çıkarlar(1). Kesin tanı ve tedavi cerrahi ile olur ve rüptür öncesi uygulanan splenektomi yaşam süresini anlamlı şekilde uzatır(5). Primer splenik anjiosarkomalı bir hastanın tanı, radyolojik patolojik bulgular ve tedavisini sunuyoruz.
Although primary splenic angiosarcomas are the most common malignant nonhematopoietic tumors of spleen(1) ,they are extremely rare tumors with very poor prognosis(2). These tumors are highly aggressive and lethal,present with widespread metastasis or splenic rupture(1). Definitive diagnosis and treatment is surgical and survival is significantly improved when splenectomy is performed prior to rupture(5). Diagnosis, radiologic and pathologic findings and treatment of a patient with primary splenic angiosarcoma is presented.</description><issn>1019-1941</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNotjMtKxDAUQLNQmHH0EwbyAVO46SPpxZWMTxhwM_tym0eNtklJ4sK_F3RWhwOHc8W2AgRWAluxYTc5fwJ0PaDcsuHR0xRi9vnAS7JUFhvKgScyPs5x8ppTMHyl8nFR54PxYco8Op7X2Ya_ZPIxU9JxoXtOXFO2PNk1pnLLrh3N2d5duGPn56fz8bU6vb-8HR9OVcZaVaMEY3oHqnbkyPR1i1pKdNRqbAQKUF2tNYIi1SMgKWcVyFFgR42EUTU7tv_ffs_0NfplWJNfKP0MAlolVPMLp0pNXw</recordid><startdate>2009</startdate><enddate>2009</enddate><creator>YALMAN, Haydar</creator><creator>YİĞİTBAŞI, Rafet</creator><creator>DEMİRAL, Gökhan</creator><creator>OKUR, Özlem</creator><creator>EVCİMİK, Taner</creator><creator>EKİNCİ, Özgür</creator><creator>AKSOY, Fikret</creator><general>Marmara Üniversitesi</general><scope>GIY</scope><scope>GIZ</scope><scope>GJA</scope><scope>GJB</scope></search><sort><creationdate>2009</creationdate><title>Diagnosis, treatment, radiologic and pathologic findings of splenic angiosarcoma; a case report</title><author>YALMAN, Haydar ; YİĞİTBAŞI, Rafet ; DEMİRAL, Gökhan ; OKUR, Özlem ; EVCİMİK, Taner ; EKİNCİ, Özgür ; AKSOY, Fikret</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-s927-b60dd8f072fafad8249c669fa4c931910752cc907a78909a7fe706b195a360b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>YALMAN, Haydar</creatorcontrib><creatorcontrib>YİĞİTBAŞI, Rafet</creatorcontrib><creatorcontrib>DEMİRAL, Gökhan</creatorcontrib><creatorcontrib>OKUR, Özlem</creatorcontrib><creatorcontrib>EVCİMİK, Taner</creatorcontrib><creatorcontrib>EKİNCİ, Özgür</creatorcontrib><creatorcontrib>AKSOY, Fikret</creatorcontrib><collection>ULAKBIM - Mühendislik ve Temel Bilimler Veri Tabani</collection><collection>ULAKBIM - Yaşam Bilimleri Veri Tabani</collection><collection>ULAKBIM - Turk Sosyal Bilimler Veri Tabani</collection><collection>ULAKBIM - Türk Tıp Veri Tabani</collection><jtitle>Marmara Medical Journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>YALMAN, Haydar</au><au>YİĞİTBAŞI, Rafet</au><au>DEMİRAL, Gökhan</au><au>OKUR, Özlem</au><au>EVCİMİK, Taner</au><au>EKİNCİ, Özgür</au><au>AKSOY, Fikret</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnosis, treatment, radiologic and pathologic findings of splenic angiosarcoma; a case report</atitle><jtitle>Marmara Medical Journal</jtitle><date>2009</date><risdate>2009</risdate><volume>22</volume><issue>1</issue><spage>56</spage><epage>58</epage><pages>56-58</pages><issn>1019-1941</issn><abstract>Primer splenik anjiosarkomalar dalağın hematopoetik sistemle ilişkili olmayan en sık malign tümörleri(1) olmasına karşın oldukça nadir görülmekte ve prognozu son derece kötüdür(2). Bu tümörlerin seyri oldukça agresif ve ölümcül olup yaygın metastazlar veya dalak rüptürü ile karşımıza çıkarlar(1). Kesin tanı ve tedavi cerrahi ile olur ve rüptür öncesi uygulanan splenektomi yaşam süresini anlamlı şekilde uzatır(5). Primer splenik anjiosarkomalı bir hastanın tanı, radyolojik patolojik bulgular ve tedavisini sunuyoruz.
Although primary splenic angiosarcomas are the most common malignant nonhematopoietic tumors of spleen(1) ,they are extremely rare tumors with very poor prognosis(2). These tumors are highly aggressive and lethal,present with widespread metastasis or splenic rupture(1). Definitive diagnosis and treatment is surgical and survival is significantly improved when splenectomy is performed prior to rupture(5). Diagnosis, radiologic and pathologic findings and treatment of a patient with primary splenic angiosarcoma is presented.</abstract><pub>Marmara Üniversitesi</pub><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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title | Diagnosis, treatment, radiologic and pathologic findings of splenic angiosarcoma; a case report |
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