Tocilizumab for the treatment of TAFRO syndrome: a systematic literature review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00277-020-04275-0.pdf
Reference65 articles.
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2. Takai K, Nikkuni K, Momoi A, Nagai K, Igarashi N, Saeki T (2013) Thrombocytopenia with reticulin fibrosis accompanied by fever, anasarca and hepatosplenomegaly: a clinical report of five cases. J Clin Exp Hematop. 53:63–68
3. Kawabata H, Takai K, Kojima M, Nakamura N, Aoki S, Nakamura S, Kinoshita T, Masaki Y (2013) Castleman-Kojima disease (TAFRO syndrome): a novel systemic inflammatory disease characterized by a constellation of symptoms, namely, thrombocytopenia, ascites (anasarca), microcytic anemia, myelofibrosis, renal dysfunction, and organomegaly: a status report and summary of Fukushima (6 June, 2012) and Nagoya meetings (22 September, 2012). J Clin Exp Hematop 53:57–61
4. Srkalovic G, Marijanovic I, Srkalovic MB, Fajgenbaum DC (2017) TAFRO syndrome: new subtype of idiopathic multicentric Castleman disease. Bosn J Basic Med Sci 17:81–84
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2. TAFRO Syndrome: Guidance for Managing Patients Presenting Thrombocytopenia, Anasarca, Fever, Reticulin Fibrosis, Renal Insufficiency, and Organomegaly;Biomedicines;2024-06-08
3. TAFRO syndrome associated with C3 nephropathy (an analysis of clinical experience);The Clinician;2024-01-19
4. Unmet Clinical Needs in the Management of Idiopathic Multicentric Castleman Disease: A Consensus-based Position Paper From an ad hoc Expert Panel;HemaSphere;2023-05-23
5. TAFRO Syndrome Mimicking Solid Cancer and Successfully Treated by Tocilizumab: A Case and Literature Review;Journal of Cancer Research and Practice;2023
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