Literature DB >> 27660586

Metastatic Cardiac Angiosarcoma in a 26-Year-Old Male.

Elizabeth S Ellent1, Ronald Chong-Yik2, Abdul Mukhtadir Khan3.   

Abstract

BACKGROUND: Cardiac angiosarcomas are an extremely rare tumor with an incidence of only 0.056%. Diagnosing this rare tumor becomes even more difficult as the presentation of cardiac angiosarcomas varies based on anatomic location. Depending on the tumor's proximity to valves, symptoms may be more consistent with heart failure, while growth throughout the conduction system may produce arrhythmias. CASE REPORT: We present the case of a young male with a significant tumor burden of cardiac angiosarcoma in his lungs whose symptoms included pleuritic chest pain and hemoptysis. This patient did not have the classic finding of right-sided heart failure; instead, his presenting complaint was hemoptysis.
CONCLUSION: The diagnostician's differential diagnosis must be broad when encountering common chief complaints, such as hemoptysis and chest pain.

Entities:  

Keywords:  Angiosarcoma; coronary arteries; heart failure; heart neoplasm; hemoptysis

Year:  2016        PMID: 27660586      PMCID: PMC5024819     

Source DB:  PubMed          Journal:  Ochsner J        ISSN: 1524-5012


  10 in total

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Journal:  Cardiovasc Pathol       Date:  2003 Sep-Oct       Impact factor: 2.185

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Authors:  E E Salcedo; G I Cohen; R D White; M B Davison
Journal:  Curr Probl Cardiol       Date:  1992-02       Impact factor: 5.200

10.  Embolic potential of cardiac tumors and outcome after resection: a case-control study.

Authors:  Andrew W Elbardissi; Joseph A Dearani; Richard C Daly; Charles J Mullany; Thomas A Orszulak; Francisco J Puga; Hartzell V Schaff
Journal:  Stroke       Date:  2008-10-23       Impact factor: 7.914

  10 in total

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