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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Autores principales: Vega S,Jorge, Rodríguez S,María de los Angeles, Vásquez G,Alejandro, Torres F,Carlos
Lenguaje:Spanish / Castilian
Publicado: Sociedad Médica de Santiago 2004
Materias:
IgA
Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872004000800012
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spelling 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
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AT vasquezgalejandro aplasiamedulartratadaexitosamenteconciclosporinaenunpacienteenhemodialisiscronica
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