Bone marrow transplantation for constitutional pure red cell aplasia

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Bone marrow transplantation for constitutional pure red cell aplasia.

Constitutional pure red cell aplasia (CPRCA) is a syndrome of failed erythropoiesis usually diagnosed within the first year of life. Four patients with CPRCA received transplants with marrow from their HLA-identical, mixed lymphocyte culture-nonreactive siblings. All patients were resistant to corticosteroid therapy and were dependent on regular red cell transfusions for at least 5 years. Three...

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High-dose intravenous methylprednisolone for constitutional pure red cell aplasia.

I read with interest the recent article by Lenarsky et al’ about bone marrow transplantation (BMT) for Diamond-Blackfan syndrome. I reported a case of constitutional pure red cell aplasia (CPRCA) refractory to conventional prednisone (2 mg/kg) administration treated with high-dose intravenous (IV) methylprednisolone (HIVMP) (30 mg/kg for 3 days, 20 mg/kg for 4 days, then subsequently 10, 5, and...

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Pure red cell aplasia of long duration complicating major ABO-incompatible bone marrow transplantation.

In 3 of 15 consecutive patients receiving a human leukocyte antigen (HLA)-identical but major ABO incompatible bone marrow transplant (BMT), pure red cell aplasia (PRA) lasting 5 to 8 months was observed. Titers of the incompatible anti-A agglutinin before infusion of the red blood cell (RBC)-depleted BMT was very high in one, and in the usual range in two patients. Decrease of agglutinin titer...

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Acquired pure red cell aplasia.

Correspondence MEDICALTJOSRNAL 559 Acquired Pure Red Cell Aplasia SIR,-May we make the following observation about your article on acquired pure red cell aplasia and its treatment with steroids (6 April, p. 3) ? A pure red cell aplasia that responded to riboflavine or prednisone has been described in African adults and in children with marasmus and kwashiorkor.' In marasmus and kwashiorkor an e...

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ژورنال

عنوان ژورنال: Blood

سال: 1988

ISSN: 0006-4971,1528-0020

DOI: 10.1182/blood.v71.1.226.bloodjournal711226