Results 101 to 110 of about 378 (110)
TAFRO subtype of idiopathic multicentric Castleman disease in a 22-year-old man. [PDF]
Rowe S +4 more
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Castleman Disease-Still More Questions than Answers: A Case Report and Review of the Literature. [PDF]
Sikora M +6 more
europepmc +1 more source
Idiopathic multicentric Castleman disease in children: a single-center retrospective analysis. [PDF]
Du J +9 more
europepmc +1 more source
[The guidelines for the diagnosis and treatment of Castleman disease in China (2025)]. [PDF]
Hematological Rare Disease Academic Group +3 more
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Iptacopan in C5 blockade refractory atypical hemolytic uremic syndrome with associated Castleman's disease: case report. [PDF]
Nguyen MD +10 more
europepmc +1 more source
A Phase Ib Investigator-Initiated Trial of Filgotinib in Patients With Idiopathic Multicentric Castleman Disease. [PDF]
Fukui S +16 more
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Idiopathic Multicentric Castleman's Disease as a Mimicker of IgG4-related Disease. [PDF]
Yoshimi R, Nakajima H.
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Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
Idiopathic multicentric Castleman disease is a rare lymphoproliferative disorder that is clinically classified into idiopathic plasmacytic lymphadenopathy (IPL); thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly (TAFRO); and not otherwise specified (NOS).
Tomoka, Haratake +11 more
openaire +1 more source
Idiopathic multicentric Castleman disease is a rare lymphoproliferative disorder that is clinically classified into idiopathic plasmacytic lymphadenopathy (IPL); thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly (TAFRO); and not otherwise specified (NOS).
Tomoka, Haratake +11 more
openaire +1 more source

