An Infant with TAFRO Syndrome: Case Report and Review of the Literature

Abstract excerpt

A rare lymphoproliferative disorder involving thrombocytopenia (T), anasarca (A), fever (F), reticulin fibrosis (R), and organomegaly (O), so called TAFRO syndrome, was first reported in 2010.1 Considered a variant of idiopathic multicentric Castleman’s disease, the recent discovery and rarity of this syndrome poses significant challenges to diagnosis and management. In this case report, we review the youngest pat...

Topics

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• Alleles
• Blood disorders and treatments
• Clinical Decision-Making
• Disease Management
• Genetic Diseases, Inborn
• Genetic Predisposition to Disease
• Germ-Line Mutation
• Practice Guidelines as Topic

Identifiers and source

Literature Corpus work

dc56471f-ca88-5e0c-b236-8f11aac5243f

DOI

10.22541/au.165035703.39925793/v1