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Published in: Annals of Hematology 3/2017

01-03-2017 | Letter to the Editor

Potential value of FDG PET-CT in diagnosis and follow-up of TAFRO syndrome

Authors: Fatemeh Behnia, Saeed Elojeimy, Manuela Matesan, David C. Fajgenbaum

Published in: Annals of Hematology | Issue 3/2017

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Excerpt

Dear Editor, …
Literature
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go back to reference Takai K, Nikkuni K, Shibuya H, Hashidate H (2010) Thrombocytopenia with mild bone marrow fibrosis accompanied by fever, pleural effusion, ascites and hepatosplenomegaly. Rinsho Ketsueki 51:320–325 (in Japanese)PubMed Takai K, Nikkuni K, Shibuya H, Hashidate H (2010) Thrombocytopenia with mild bone marrow fibrosis accompanied by fever, pleural effusion, ascites and hepatosplenomegaly. Rinsho Ketsueki 51:320–325 (in Japanese)PubMed
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go back to reference Kojima M, Nakamura N, Tsukamoto N, Yokohama A, Itoh H, Kobayashi S, Kashimura M, Masawa N, Nakamura S (2011) Multicentric Castleman’s disease representing effusion at initial clinical presentation: clinicopathological study of seven cases. Lupus 20(1):44–50CrossRefPubMed Kojima M, Nakamura N, Tsukamoto N, Yokohama A, Itoh H, Kobayashi S, Kashimura M, Masawa N, Nakamura S (2011) Multicentric Castleman’s disease representing effusion at initial clinical presentation: clinicopathological study of seven cases. Lupus 20(1):44–50CrossRefPubMed
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go back to reference Kojima M, Nakamura N, Tsukamoto N et al (2008) Clinical implications of idiopathic multicentric Castleman disease among Japanese: a report of 28 cases. Int J Surg Pathol 16:391–398CrossRefPubMed Kojima M, Nakamura N, Tsukamoto N et al (2008) Clinical implications of idiopathic multicentric Castleman disease among Japanese: a report of 28 cases. Int J Surg Pathol 16:391–398CrossRefPubMed
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go back to reference 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(1):57–61. doi:10.3960/jslrt.53.57 CrossRefPubMed 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(1):57–61. doi:10.​3960/​jslrt.​53.​57 CrossRefPubMed
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Metadata
Title
Potential value of FDG PET-CT in diagnosis and follow-up of TAFRO syndrome
Authors
Fatemeh Behnia
Saeed Elojeimy
Manuela Matesan
David C. Fajgenbaum
Publication date
01-03-2017
Publisher
Springer Berlin Heidelberg
Published in
Annals of Hematology / Issue 3/2017
Print ISSN: 0939-5555
Electronic ISSN: 1432-0584
DOI
https://doi.org/10.1007/s00277-016-2875-8

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