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Br J Haematol ; 121(1): 119-22, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12670341

ABSTRACT

The tendency for thrombosis to occur if haemolysis persists after splenectomy is especially marked in "hereditary stomatocytosis", in which the red cell membrane "leaks" Na and K. A 21-year-old woman, who was splenectomized in childhood for a congenital haemolytic state, presented with major pulmonary embolism that recurred despite anticoagulation. Tests showed a significant cation leak with a "shallow-slope" abnormality in temperature dependence. Allogeneic bone marrow transplantation caused the thrombophilic state to cease and subsequently anticoagulation was stopped without recurrence of thromboembolism. However, she died 9 months after transplantation: iron overload, intensified by the transfusion demands of the transplant, was a major factor.


Subject(s)
Anemia, Hemolytic/therapy , Bone Marrow Transplantation , Thrombophilia/therapy , Adult , Anemia, Hemolytic/metabolism , Anemia, Hemolytic/surgery , Erythrocyte Membrane/metabolism , Fatal Outcome , Female , Humans , Iron Overload , Potassium/metabolism , Pulmonary Embolism/etiology , Pulmonary Embolism/metabolism , Sodium/metabolism , Splenectomy , Thrombophilia/metabolism , Transplantation, Homologous
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