TAFRO syndrome: A case report and review of the literature

TAFRO syndrome is a rare clinicopathologic variant of idiopathic multicentric Castleman disease characterized by Thrombocytopenia, Ascites (anasarca), myeloFibrosis, Renal dysfunction, and Organomegaly. Here, we report a case of TAFRO syndrome in an HIV-negative young Caucasian male who presented wi...

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Publicado en:Hum Pathol (N Y)
Main Authors: Hou, Tieying, Dhillon, Jaspreet, Xiao, Wenbin, Jaffe, Elaine S., Sands, Amy M., Neppalli, Vishala, Deeb, George, Zhang, Nan
Formato: Artigo
Idioma:Inglês
Publicado: 2017
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6787913/
https://ncbi.nlm.nih.gov/pubmed/31608209
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ehpc.2017.04.003
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