Concurrent primary pneumococcemia, disseminated intravascular coagulation, and sickle cell anemia

Fulminant pneumococcal infections are rare in teen-agers with sickle cell anemia. A 16-year-old black male with sickle cell anemia was treated as an outpatient for cryptogenic pain crisis, which delayed antibiotic therapy for primary pneumococcal septicemia for seven hours. This patient did not appe...

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Veröffentlicht in:Southern medical journal (Birmingham, Ala.) Ala.), 1978-07, Vol.71 (7), p.858-859
Hauptverfasser: McDonald, C R, Eichner, E R
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container_title Southern medical journal (Birmingham, Ala.)
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creator McDonald, C R
Eichner, E R
description Fulminant pneumococcal infections are rare in teen-agers with sickle cell anemia. A 16-year-old black male with sickle cell anemia was treated as an outpatient for cryptogenic pain crisis, which delayed antibiotic therapy for primary pneumococcal septicemia for seven hours. This patient did not appear ill upon initial presentation but rapidly developed disseminated intravascular coagulation and died.
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identifier ISSN: 0038-4348
ispartof Southern medical journal (Birmingham, Ala.), 1978-07, Vol.71 (7), p.858-859
issn 0038-4348
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source MEDLINE; Journals@Ovid Complete
subjects Adolescent
Anemia, Sickle Cell - complications
Anemia, Sickle Cell - immunology
Disseminated Intravascular Coagulation - complications
Humans
Male
Pneumococcal Infections - complications
Sepsis - complications
Sepsis - etiology
title Concurrent primary pneumococcemia, disseminated intravascular coagulation, and sickle cell anemia
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