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 CASE REPORT
Year : 2002  |  Volume : 48  |  Issue : 1  |  Page : 37-8

Acquired pure red cell aplasia in a child.


Division of Paediatric Haematology-Oncology, L.T.M.G. Hospital, Sion, Mumbai - 400022, India., India

Correspondence Address:
R A Sharma
Division of Paediatric Haematology-Oncology, L.T.M.G. Hospital, Sion, Mumbai - 400022, India.
India
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Source of Support: None, Conflict of Interest: None


PMID: 12082327

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Primary acquired pure red cell aplasia is a rare occurrence in childhood. An eleven-year old boy presented to us with pallor, which required multiple packed red cell transfusions. He did not have hepatosplenomegaly, jaundice or lymphadenopathy. Bone marrow examination revealed the diagnosis of pure red cell aplasia. All possible investigations were done to exclude secondary causes of pure red cell aplasia. No secondary cause was found on investigations. Rheumatoid factor and anti-nuclear antibodies were positive. He was started on oral steroids, to which he did not respond. He was then given cyclosporine A. Response to cyclosporine was dramatic and the child now does not require any transfusions.






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Online since 12th February '04
2004 - Journal of Postgraduate Medicine
Official Publication of the Staff Society of the Seth GS Medical College and KEM Hospital, Mumbai, India
Published by Wolters Kluwer - Medknow