HepaticCampylobacter jejuniinfection in patients with Castleman‐Kojima disease (idiopathic multicentric Castleman disease with thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly (TAFRO) syndrome)
Abstract
Castleman‐Kojima disease, also known as idiopathic multicentric Castleman disease with TAFRO syndrome (iMCD‐TAFRO), is a recently recognized systemic inflammatory disorder with a characteristic series of clinical symptoms, including thrombocytopenia (T), anasarca (A), fever (F), reticulin fibrosis (R), and organomegaly (O). Patients with iMCD‐TAFRO often develop severe abdominal pain, elevated alkaline phosphatase levels, and systemic...
Paper Details
Title
HepaticCampylobacter jejuniinfection in patients with Castleman‐Kojima disease (idiopathic multicentric Castleman disease with thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly (TAFRO) syndrome)
Published Date
Oct 1, 2019
Journal
Volume
69
Issue
10
Pages
572 - 579
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