Sudden Unexpected Death in a Patient with Splenic Sequestration and Sickle Cell-β+-thalassemia Syndrome

    Volume 46, Issue 2 (March 2001)

    ISSN: 0022-1198

    CODEN: JFSOAD

    Page Count: 3


    Phatak, D
    University of Medicine and Dentistry, State of New Jersey Medical School, Newark, NJ

    Natarajan, GA

    Hutchins, KD
    Associate medical examiner and regional medical examiner, Regional Medical Examiner Office, Edwin H. Albano Institute of Forensic Sciences, Newark, NJ

    Ballas, SK
    Professor of Medicine and Pediatrics, Cardeza Foundation for Hematologic Research, Jefferson Medical College, Philadelphia, PA

    (Received 30 November 1999; accepted 10 April 2000)

    Abstract

    Acute splenic sequestration crisis is a rare disorder that usually occurs in children, with sickle cell anemia, who are under the age of five years. A few cases have been described in adults with heterozygous sickle cell syndromes. Though this entity can be fatal there have been no reported cases associated with sudden death. We describe a case of sudden, unexpected death, associated with splenic sequestration, in a 29-year-old African-American man with undiagnosed sickle cell-β+-thalassemia syndrome.


    Paper ID: JFS14985J

    DOI: 10.1520/JFS14985J

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    Title Sudden Unexpected Death in a Patient with Splenic Sequestration and Sickle Cell-β+-thalassemia Syndrome
    Symposium , 0000-00-00
    Committee E30