RESUMO
We describe the case of a 20-year-old man who developed severe thrombocytopenia and hemorrhagic complications 5 months after beginning pegylated interferon therapy for chronic hepatitis C. Interferon therapy was stopped and platelets were transfused, but the platelet count did not increase until treatment with immunoglobulins and intravenous corticosteroids was started. Therefore, we believe this would suggest a possible autoimmune mechanism for the development of thrombocytopenia with interferon therapy. Mild reduction in platelets count is a common adverse effect of this drug. Nevertheless, severe decreases and secondary serious hemorrhagic complications have been infrequently described in the literature.
Assuntos
Antivirais/efeitos adversos , Hepatite C Crônica/tratamento farmacológico , Interferons/efeitos adversos , Polietilenoglicóis/efeitos adversos , Púrpura Trombocitopênica Idiopática/induzido quimicamente , Adulto , Antivirais/administração & dosagem , Antivirais/uso terapêutico , Terapia Combinada , Quimioterapia Combinada , Transtornos Hemorrágicos/etiologia , Hepatite C Crônica/complicações , Humanos , Imunoglobulinas Intravenosas , Interferons/administração & dosagem , Interferons/uso terapêutico , Masculino , Metilprednisolona/uso terapêutico , Transfusão de Plaquetas , Polietilenoglicóis/administração & dosagem , Polietilenoglicóis/uso terapêutico , Púrpura Trombocitopênica Idiopática/tratamento farmacológico , Púrpura Trombocitopênica Idiopática/terapia , Ribavirina/administração & dosagem , Ribavirina/uso terapêuticoRESUMO
Acquired erythroblastopenia, or pure red cell aplasia, may appear as a complication of chronic lymphocytic leukaemia. This was the case in a 58 year-old man, diagnosed as having B-cell chronic lymphocytic leukaemia considered as stage C (III). He was treated initially with chlorambucil; two months after diagnosis the patient showed erythroblastopenia, being treated with chlorambucil-prednisone, cyclophosphamide-prednisone, prednisone alone, and intravenous immunoglobulins. No satisfactory response was achieved with any of these drugs. During a period of 28 weeks the patient received 41 units of packed red cells. Cyclosporin-A, at a 9 mg/Kg daily doses, was tested, a dramatic response being observed: after four weeks of such therapy the patient's haemoglobin reached 14.5 g/dL, and he needed no further transfusion since the beginning of this treatment.