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Detection of Residual Donor Erythroid Progenitor Cells after Hematopoietic Stem Cell Transplantation for Patients with Hemoglobinopathies
Published on: September 6, 2017
Pure red cell aplasia and adult-onset Still's disease
Jae-Wook Chung1, Yu-Jin Suh, Hyun-Ju Song
1Department of Allergy-Rheumatology, Ajou University School of Medicine, Paldal-gu, Suwon, Korea.
Abstract:
Pure red cell aplasia (PRCA) associated with adult-onset Still's disease (AOSD) is very rare. In this report a 28-year-old woman was admitted with fever, skin rash, jaundice and anemia. She was diagnosed as having AOSD with PRCA by bone marrow examination. Treatment with high-dose prednisolone and intravenous immunoglobulin resulted in remission of the PRCA and a good response of the AOSD.
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