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The first report of adolescent TAFRO syndrome, a unique clinicopathologic variant of multicentric Castleman’s disease

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TAFRO syndrome is a unique clinicopathologic variant of multicentric Castleman’s disease that has recently been identified in Japan. It is characterized by a constellation of symptoms: Thrombocytopenia, Anasarca, reticulin Fibrosis of the bone marrow, Renal dysfunction and Organomegaly (TAFRO). | The first report of adolescent TAFRO syndrome, a unique clinicopathologic variant of multicentric Castleman’s disease

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