Thrombocytopenia, anasarca, fever, reticulin fibrosis, renal insufficiency, and organomegaly
(TAFRO) syndrome is a heterogeneous entity manifesting with a constellation of symptoms …

Background Sjögren's syndrome (SjS) is a systemic autoimmune disease characterized by
lymphocytic infiltration of the salivary and lacrimal glands associated with sicca syndrome …

TAFRO syndrome is an acute systemic inflammatory disease characterized by
thrombocytopenia, anasarca, fever, reticulin fibrosis/renal dysfunction, and organomegaly …

Disseminated intravascular coagulation (DIC) is a common complication in sepsis. Since
DIC not only promotes organ dysfunction but also is a strong prognostic factor, its diagnosis …

The term multicentric Castleman disease (MCD) encompasses a spectrum of conditions that
share some overlapping clinicopathological manifestations. The fundamental pathogenetic …

TAFRO syndrome is a systemic inflammatory disorder of unknown etiology characterized by
thrombocytopenia, anasarca, fever, reticulin myelofibrosis, renal dysfunction, and …

Since thrombocytopenia, anasarca, fever, reticulin fibrosis, renal insufficiency, and
organomegaly (TAFRO) syndrome was first proposed in 2010, there has been considerable …

Background: TAFRO syndrome is a clinical subtype of idiopathic multicentric Castleman
disease (iMCD) that is characterized by thrombocytopenia, anasarca, fever and/or elevated …

Thrombocytopenia, anasarca, fever, reticulin fibrosis/renal failure, and organomegaly
(TAFRO) syndrome is rare in clinical practice. It is a systemic inflammatory disease caused …

TAFRO syndrome is a newly recognized disease entity characterized by thrombocytopenia,
anasarca, fever, reticulin myelofibrosis, renal dysfunction, and organomegaly. The objective …