Acquired amegakaryocytic thrombocytopenia and pure red cell aplasia associated with an occult large granular lymphocyte leukemia
β Scribed by Dominic W. Lai; Thomas P. Loughran Jr.; Jaroslaw P. Maciejewski; Sebastian Sasu; Sophie X. Song; P.K. Epling-Burnette; Ronald L. Paquette
- Book ID
- 104040526
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- English
- Weight
- 756 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0145-2126
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Neoplastic disorders sometimes accompany a renal transplant. Herein, we report a large granular lymphocyte (LGL) leukemia patient with pure red cell aplasia (PRCA) after renal transplantation. A 36-year-old female was presented to our department with anemia in February 1996. She had undergone hemodi
## Abstract We present a female patient with TβΞ³ LGL leukemia, who was followed for the last 20 years. Over these years she developed several autoimmune disorders, including SjΓΆgren's syndrome, Hashimoto's thyroiditis, premature ovarian failure (compatible with type II autoimmune polyglandular synd
To the Editor: Semenzato et al. proposed new criteria for large granular lymphocyte (LGL) leukemia because patients with low levels of GL were similar to those with levels greater than 2,000 GL/l [1]. LGL leukemia is a GL proliferative disease often accompanied by pure red cell aplasia (PRCA). T-cel