Volume 37, Issue 5 (September 1992)

    Fatal Virus-Associated Hemophagocytic Syndrome in a Young Adult Producing Nontraumatic Splenic Rupture

    (Received 9 January 1992; accepted 10 February 1992)

    CODEN: JFSOAD

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    Abstract

    A 24-year-old man with no previous medical history was admitted to a local hospital with pancytopenia after a recent “viral illness.” During his hospitalization, he developed sudden abdominal distension and hypotension. Surgical exploration of his abdomen revealed a ruptured spleen. The spleen was removed, but the patient did not survive the operation. We investigated this unexpected and unexplained hospital death for any traumatic or iatrogenic injury. The cause of death after review of the clinical history, autopsy, and microscopic sections was virus-associated hemophagocytic syndrome (VAHS). VAHS consists of a generalized histiocytic proliferation and marked hemophagocytosis associated with a systemic viral infection. Clinically it presents as pancytopenia and organomegaly. This recently described entity is often confused with malignant histiocytosis. This is the first case report of VAHS producing nontraumatic splenic rupture, thus adding to the differential diagnosis of spontaneous splenic rupture and sudden natural death.


    Author Information:

    Bell, MD
    Associate Medical Examiner, Broward County Medical Examiner's Office, University of Miami School of Medicine/Dept. of Pathology, Ft. Lauderdale, FL

    Wright, RK
    Chief Medical Examiner, Broward County Medical Examiner's Office, University of Miami School of Medicine/Dept. of Pathology, Ft. Lauderdale, FL


    Stock #: JFS13332J

    ISSN: 0022-1198

    DOI: 10.1520/JFS13332J

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    Author
    Title Fatal Virus-Associated Hemophagocytic Syndrome in a Young Adult Producing Nontraumatic Splenic Rupture
    Symposium , 0000-00-00
    Committee E30