Hemophilic splenic rupture without thrombocytosis

Spontaneous splenic rupture in hemophilia A is an uncommon occurrence which is difficult to diagnose. We have reported a case of hemophilic rupture of the spleen unaccompanied by thrombocytosis, which has been emphasized as a diagnostic clue to hemophilic splenic rupture. Hence, splenic rupture shou...

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Veröffentlicht in:Southern medical journal (Birmingham, Ala.) Ala.), 1983-02, Vol.76 (2), p.272-272
Hauptverfasser: Krauss, J S, Hahn, D A
Format: Artikel
Sprache:eng
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Zusammenfassung:Spontaneous splenic rupture in hemophilia A is an uncommon occurrence which is difficult to diagnose. We have reported a case of hemophilic rupture of the spleen unaccompanied by thrombocytosis, which has been emphasized as a diagnostic clue to hemophilic splenic rupture. Hence, splenic rupture should still be considered in any hemophilic patient with pain in the left upper quadrant and a normal platelet count. Splenic rupture in hemophilia must be recognized because its treatment requires not only clotting factor infusion but also surgical intervention.
ISSN:0038-4348
DOI:10.1097/00007611-198302000-00040