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10.5114/aoms.2014.40741 http://scihub22266oqcxt.onion/10.5114/aoms.2014.40741 24701226/?report=reader!3953983!24701226     free     free     free Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Arch+Med+Sci 2014 ; 10 (1): 135-48 Nephropedia Template TP {{tp|p=24701226|t=2014. Sarcomas of the heart as a difficult interdisciplinary problem |pdf=|usr=}}{{24701226}} gab.com Text Sarcomas of the heart as a difficult interdisciplinary problem JO: Arch Med Sci http://www.kidney.de/pget.php?&tw=1&pmid=24701226 #FOAvip Cardiac tumors are assumed to be a rare entity. Metastases to the heart are more frequent than primary lesions. Sarcomas make up the majority of cardiac malignant neoplasms. Among them angiosarcoma is the most common and associated with the worst prognosis. Malignant fibrous histiocytoma comprises the minority of cardiac sarcomas and has uncertain etiology as well as pathogenesis. Transthoracic echocardiography remains the widely available screening examination for the initial diagnosis of a cardiac tumor. The clinical presentation is non-specific and the diagnosis is established usually at an advanced stage of the disease. Sarcomas spread preferentially through blood due to their immature vessels without endothelial lining. Surgery remains the method of choice for treatment. Radicalness of the excision is still the most valuable prognostic factor. Adjuvant therapy is unlikely to be effective. The management of cardiac sarcomas must be individualized due to their rarity and significant differences in the course of disease. Twit Text FOAVip Sarcomas of the heart as a difficult interdisciplinary problem ????Arch Med Sci http://www.kidney.de/pget.php?&tw=1&pmid=24701226 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24701226 #FOAvip English Wikipedia <ref>{{Cite pmid|24701226}}</ref> Sarcomas of the heart as a difficult interdisciplinary problem #MMPMID24701226 Ostrowski S; Marcinkiewicz A; Kosmider A; Jaszewski R Arch Med Sci 2014[Feb]; 10 (1): 135-48 PMID24701226show ga Cardiac tumors are assumed to be a rare entity. Metastases to the heart are more frequent than primary lesions. Sarcomas make up the majority of cardiac malignant neoplasms. Among them angiosarcoma is the most common and associated with the worst prognosis. Malignant fibrous histiocytoma comprises the minority of cardiac sarcomas and has uncertain etiology as well as pathogenesis. Transthoracic echocardiography remains the widely available screening examination for the initial diagnosis of a cardiac tumor. The clinical presentation is non-specific and the diagnosis is established usually at an advanced stage of the disease. Sarcomas spread preferentially through blood due to their immature vessels without endothelial lining. Surgery remains the method of choice for treatment. Radicalness of the excision is still the most valuable prognostic factor. Adjuvant therapy is unlikely to be effective. The management of cardiac sarcomas must be individualized due to their rarity and significant differences in the course of disease. äSarcomas of the heart as a difficult interdisciplinary problem (epmc).pdf DeepDyve Pubget Overpricing