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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 gai...

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Podrobná bibliografie
Vydáno v:Front Immunol
Hlavní autoři: Leurs, Amélie, Gnemmi, Viviane, Lionet, Arnaud, Renaud, Loïc, Gibier, Jean-Baptiste, Copin, Marie-Christine, Hachulla, Eric, Hatron, Pierre-Yves, Launay, David, Fajgenbaum, David, Terriou, Louis
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2019
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6609882/
https://ncbi.nlm.nih.gov/pubmed/31316523
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2019.01489
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