Sudden Unexpected Death in Young Adult due to Right Ventricular Dysplasia

    Volume 42, Issue 1 (January 1997)

    ISSN: 0022-1198

    CODEN: JFSOAD

    Page Count: 3


    Lane, CD
    Pathologist, The Reading Hospital and Medical Center, Reading, PA

    (Received 1 April 1996; accepted 15 May 1996)

    Abstract

    This case report illustrates a rare familial cardiomyopathy first reported in the medical literature in 1982 known as right ventricular dysplasia (right ventricular cardiomyopathy). The patient is a young woman with a history of cardiac arrhythmias suspected to be associated with prolapsed mitral valve who presented to the Berks County Coroner's office as a sudden unexpected death in a young adult. It is important to recognize the illustrated classic cardiac pathology of this rare entity for clinical management, as an anatomic explanation of cause of sudden death and for the accumulation of statistics to establish frequency, conditions of predisposition, response to therapy and predicted outcome.


    Paper ID: JFS14086J

    DOI: 10.1520/JFS14086J

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    Author
    Title Sudden Unexpected Death in Young Adult due to Right Ventricular Dysplasia
    Symposium , 0000-00-00
    Committee E30