Aplasia medular tratada exitosamente con ciclosporina en un paciente en hemodiálisis crónica
A 28 years old male on chronic hemodialysis for 40 months due to a IgA crescentic glomerulonephritis developed pancytopenia (hematocrit 16%, white blood cell count 3.800 mm³ and platelets 11.000 mm³. The bone marrow aspirate showed erythropoietic hyperplasia. Hemolytic anemia, folate or vitamin B12...
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Sociedad Médica de Santiago
2004
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oai:scielo:S0034-988720040008000122014-08-14Aplasia medular tratada exitosamente con ciclosporina en un paciente en hemodiálisis crónicaVega S,JorgeRodríguez S,María de los AngelesVásquez G,AlejandroTorres F,Carlos Anemia, aplastic Bone marrow Glomerulonephritis IgA Pancytopenia A 28 years old male on chronic hemodialysis for 40 months due to a IgA crescentic glomerulonephritis developed pancytopenia (hematocrit 16%, white blood cell count 3.800 mm³ and platelets 11.000 mm³. The bone marrow aspirate showed erythropoietic hyperplasia. Hemolytic anemia, folate or vitamin B12 deficiency and paroxysmal nocturnal hemoglobinuria were ruled out. Steroids were given with a transient elevation of red cells and platelets, which lasted only for some weeks. Afterwards, intravenous immunoglobulin was given without benefit. Two months after, a bone marrow biopsy and a bone marrow magnetic resonance imaging showed severe aplasia. Cyclosporine was started with a rapid increase in blood cells count. Eight months later, he received a renal transplant from a cadaveric donor. Immunosupression was achieved with cyclosporine, prednisone and mycofenolate mofetil. The patient required hemodialysis for the first three weeks and a mild acute cellular rejection was treated with methylprednisolone. At discharge, 6 weeks later, serum creatinine was 2.4 mg/dl and creatinine clearance 37.6 ml/min. During the first months after transplant, platelet count and hemoglobin decreased and a bone marrow biopsy showed only mild hypoplasia. Four months after renal transplant the hematocrit was 43%, white blood cell count 6.600 mm³ and platelets, 150.000 mm³ and did not change during the first year of follow up (Rev Méd Chile 2004; 132: 989-94info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.132 n.8 20042004-08-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872004000800012es10.4067/S0034-98872004000800012 |
institution |
Scielo Chile |
collection |
Scielo Chile |
language |
Spanish / Castilian |
topic |
Anemia, aplastic Bone marrow Glomerulonephritis IgA Pancytopenia |
spellingShingle |
Anemia, aplastic Bone marrow Glomerulonephritis IgA Pancytopenia Vega S,Jorge Rodríguez S,María de los Angeles Vásquez G,Alejandro Torres F,Carlos Aplasia medular tratada exitosamente con ciclosporina en un paciente en hemodiálisis crónica |
description |
A 28 years old male on chronic hemodialysis for 40 months due to a IgA crescentic glomerulonephritis developed pancytopenia (hematocrit 16%, white blood cell count 3.800 mm³ and platelets 11.000 mm³. The bone marrow aspirate showed erythropoietic hyperplasia. Hemolytic anemia, folate or vitamin B12 deficiency and paroxysmal nocturnal hemoglobinuria were ruled out. Steroids were given with a transient elevation of red cells and platelets, which lasted only for some weeks. Afterwards, intravenous immunoglobulin was given without benefit. Two months after, a bone marrow biopsy and a bone marrow magnetic resonance imaging showed severe aplasia. Cyclosporine was started with a rapid increase in blood cells count. Eight months later, he received a renal transplant from a cadaveric donor. Immunosupression was achieved with cyclosporine, prednisone and mycofenolate mofetil. The patient required hemodialysis for the first three weeks and a mild acute cellular rejection was treated with methylprednisolone. At discharge, 6 weeks later, serum creatinine was 2.4 mg/dl and creatinine clearance 37.6 ml/min. During the first months after transplant, platelet count and hemoglobin decreased and a bone marrow biopsy showed only mild hypoplasia. Four months after renal transplant the hematocrit was 43%, white blood cell count 6.600 mm³ and platelets, 150.000 mm³ and did not change during the first year of follow up (Rev Méd Chile 2004; 132: 989-94 |
author |
Vega S,Jorge Rodríguez S,María de los Angeles Vásquez G,Alejandro Torres F,Carlos |
author_facet |
Vega S,Jorge Rodríguez S,María de los Angeles Vásquez G,Alejandro Torres F,Carlos |
author_sort |
Vega S,Jorge |
title |
Aplasia medular tratada exitosamente con ciclosporina en un paciente en hemodiálisis crónica |
title_short |
Aplasia medular tratada exitosamente con ciclosporina en un paciente en hemodiálisis crónica |
title_full |
Aplasia medular tratada exitosamente con ciclosporina en un paciente en hemodiálisis crónica |
title_fullStr |
Aplasia medular tratada exitosamente con ciclosporina en un paciente en hemodiálisis crónica |
title_full_unstemmed |
Aplasia medular tratada exitosamente con ciclosporina en un paciente en hemodiálisis crónica |
title_sort |
aplasia medular tratada exitosamente con ciclosporina en un paciente en hemodiálisis crónica |
publisher |
Sociedad Médica de Santiago |
publishDate |
2004 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872004000800012 |
work_keys_str_mv |
AT vegasjorge aplasiamedulartratadaexitosamenteconciclosporinaenunpacienteenhemodialisiscronica AT rodriguezsmariadelosangeles aplasiamedulartratadaexitosamenteconciclosporinaenunpacienteenhemodialisiscronica AT vasquezgalejandro aplasiamedulartratadaexitosamenteconciclosporinaenunpacienteenhemodialisiscronica AT torresfcarlos aplasiamedulartratadaexitosamenteconciclosporinaenunpacienteenhemodialisiscronica |
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