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Severe anemia due to transient pure red cell aplasia in early childhood

✍ Scribed by W. Tillmann; G. Prindull; W. Schröter


Publisher
Springer
Year
1976
Tongue
English
Weight
600 KB
Volume
123
Category
Article
ISSN
0340-6997

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✦ Synopsis


Five patients, 11 months to 3 4/12 years old with severe normochromic, normocytis anemia and reticulocytopenia are reported. At the height of erythropoietic arrest when erythroid precursor cells were completely absent, undifferentiated stem cells (transitional cells), accumulated in the bone marrow. They disappeared again upon spontaneous resumption of erythropoiesis. We suggest that the erythropoietic arrest had occurred at the level of the hematopoietic stem cell. All patients recovered within 1 week of diagnosis. No steroid therapy was given. Failure to recognize this clinical entity leads to unnecessary diagnostic and therapeutic procedures including the transfusion of blood.


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Transient response of pure red cell apla
✍ Dr. William Hocking; Richard Champlin; Ronald Mitsuyasu 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 English ⚖ 484 KB 👁 3 views

Pure red cell aplasia (PRCA) is an unusual complication of chronic lymphoproliferative disorders. A patient with T-cell chronic lymphocytic leukemia (T-CLL) had severe anemia and neutropenia. Initial in vitro studies demonstrated no evidence of T-cell suppression of erythropoiesis. Sequential bone m