Diamond-Blackfan anemia with very late and fatal onset aplasia in a 55-year-old patient with RPL11 mutation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00277-023-05553-3.pdf
Reference10 articles.
1. Wu X, Cheng L, Liu X, Sun Y, Li B, He G, Li J (2022) Clinical characteristics and outcomes of 100 adult patients with pure red cell aplasia. Ann Hematol 101(7):1493–1498. https://doi.org/10.1007/s00277-022-04847-2
2. Vlachaki E, Diamantidis MD, Klonizakis P, Haralambidou-Vranitsa S, Ioannidou-Papagiannaki E, Klonizakis I (2012) Pure red cell aplasia and lymphoproliferative disorders: an infrequent association. ScientificWorldJournal 2012:475313. https://doi.org/10.1100/2012/475313
3. Gurnari C, Maciejewski JP (2021) How I manage acquired pure red cell aplasia in adults. Blood 137(15):2001–2009. https://doi.org/10.1182/blood.2021010898
4. Shimazu Y, Mizumoto C, Chonabayashi K, Hanyu Y, Kanda J, Takaori-Kondo A (2023) Successful treatment with cyclosporine of pure red cell aplasia induced by obinutuzumab bendamustine therapy. Ann Hematol 102(8):2291–2292. https://doi.org/10.1007/s00277-023-05215-4
5. Means RT Jr (2016) Pure red cell aplasia. Blood 128(21):2504–2509. https://doi.org/10.1182/blood-2016-05-717140
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