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1.
An Med Interna ; 11(7): 341-4, 1994 Jul.
Article in Spanish | MEDLINE | ID: mdl-7981362

ABSTRACT

Evan's Syndrome (ES) may develop in isolation or associated to other autoimmune diseases, solid tumors and lymphoproliferative syndromes. This type of processes can be refractory to the usual medication, that is, to corticoids and splenectomy. High doses of Immunoglobulins (polyvalent IgG) and immunosuppressive drugs are therapeutical alternatives that have been used with different results. We present a case of idiopathic ES refractory to high doses of corticoids and IgG, showing complete remission after the administration of two infusions of vinblastin. We believe that vinblastin is a very useful therapeutical alternative in the cases of ES refractory to the usual treatment.


Subject(s)
Anemia, Hemolytic, Autoimmune/drug therapy , Purpura, Thrombocytopenic, Idiopathic/drug therapy , Vinblastine/therapeutic use , Aged , Female , Humans , Remission Induction , Syndrome
3.
Acta Haematol ; 82(4): 197-200, 1989.
Article in English | MEDLINE | ID: mdl-2511722

ABSTRACT

The hemophagocytic syndrome is a reactive disorder of the mononuclear phagocytic system. Most of the cases are rare complications of common infectious and neoplastic diseases, although there may be an underlying immune disorder predisposing to this syndrome. We report a case in association with immune thrombocytopenia and hemolytic anemia (Evans' syndrome). The hemophagocytic reaction appeared after a bacterial infection of the urinary tract and presented with abrupt pancytopenia and complete hemopoietic failure. We discuss the possible mechanisms of bone marrow failure related with the hemophagocytic syndrome.


Subject(s)
Bone Marrow Diseases/etiology , Escherichia coli Infections/complications , Histiocytosis, Non-Langerhans-Cell/complications , Aged , Anemia, Hemolytic/complications , Female , Histiocytosis, Non-Langerhans-Cell/etiology , Humans , Thrombocytopenia/complications
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