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Renal Pathologic Findings in TAFRO Syndrome: Is There a Continuum Between Thrombotic Microangiopathy and Membranoproliferative Glomerulonephritis? A Case Report and Literature Review

Background: TAFRO syndrome is a clinical subtype of idiopathic multicentric Castleman disease (iMCD) that is characterized by thrombocytopenia, anasarca, fever and/or elevated serum C-reactive protein, renal dysfunction, and organomegaly.Case Presentation: A 28-year-old woman with fever, weight gain...

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Detalhes bibliográficos
Main Authors: Amélie Leurs, Viviane Gnemmi, Arnaud Lionet, Loïc Renaud, Jean-Baptiste Gibier, Marie-Christine Copin, Eric Hachulla, Pierre-Yves Hatron, David Launay, David Fajgenbaum, Louis Terriou
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2019-06-01
Colecção:Frontiers in Immunology
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Acesso em linha:https://www.frontiersin.org/article/10.3389/fimmu.2019.01489/full
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