Results 41 to 50 of about 1,018 (169)
Idiopathic multicentric Castleman disease: a mysterious case of generalized lymphadenopathy [PDF]
Castleman disease is a syndrome with significant clinico-pathological overlap between malignancy, autoimmune causes and infectious etiologies.
J., Kumanan +5 more
core +2 more sources
TAFRO Syndrome with Massive Bilateral Adrenal Hemorrhage. [PDF]
Kobayashi T +12 more
europepmc +3 more sources
Borderline Case of TAFRO Syndrome and POEMS Syndrome
TAFRO syndrome and POEMS syndrome are lymphoproliferative disorders with elevated interleukin-6 and vascular endothelial growth factor (VEGF) levels; however, their underlying pathogenic mechanisms remain unclear. Similarities have been reported in the pathological findings of the lymph nodes of TAFRO syndrome, Multicentric Castleman disease (MCD), and
Shibata, Sho +9 more
openaire +3 more sources
TAFRO Syndrome With Kidney Involvement: A Case Series of Patients With Kidney Biopsies
TAFRO (thrombocytopenia, anasarca, fever, reticulin myelofibrosis/renal insufficiency, and organomegaly) syndrome is a systemic inflammatory disease sharing some features with Castleman disease and POEMS (polyneuropathy, organomegaly, endocrinopathy ...
Keiki Shimada +11 more
doaj +1 more source
TAFRO syndrome: a case report [PDF]
A man diagnosed as TAFRO syndrome was successfully responded to a novel immunosuppressive regimen containing methylprednisolone and mycophenolate mofetil. Blood cells firstly recovered, followed by the general situation and complete recover 1 month later, highlighting the danger of TAFRO syndrome and the importance of immunosuppressive agents in ...
Shan Meng +7 more
openaire +1 more source
Glomeruloid Hemangioma in a Patient with TAFRO Syndrome. [PDF]
Osano K, Hanai S, Takahashi K, Furuya F.
europepmc +4 more sources
Castleman disease (CD) is a rare lymphoproliferative disorder with multiple subtypes. Thrombocytopenia, anasarca, fever, reticulin fibrosis or renal insufficiency, and organomegaly (TAFRO) syndrome can occur in the context of CD.
Yoshito Nishimura +5 more
doaj +1 more source
Idiopathic Plasmacytic Lymphadenopathy Forms an Independent Subtype of Idiopathic Multicentric Castleman Disease [PDF]
Idiopathic multicentric Castleman disease (iMCD) is a type of Castleman disease that is not related to KSHV/HHV8 infection. Currently, iMCD is classified into iMCD-TAFRO (thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly) and iMCD ...
Maehama, Kanna +8 more
core +2 more sources
Severe systemic inflammation mimicking TAFRO syndrome following COVID-19. [PDF]
TAFRO syndrome is a rare systemic inflammatory disease. Its pathogenesis mainly involves excessive cytokine secretion and autoimmune dysfunction. Although its etiology is unclear, some viral infections have been reported to cause it. Here, we report a case of severe systemic inflammation mimicking TAFRO syndrome that arose after COVID-19.
Tane M +12 more
europepmc +3 more sources
TAFRO syndrome with renal biopsy successfully treated with steroids and cyclosporine: a case report
Background TAFRO syndrome is an acute or subacute systemic inflammatory disease with no apparent cause, presenting with fever, generalized edema, thrombocytopenia, renal damage, anemia, and organ enlargement.
Takahide Iwasaki +7 more
doaj +1 more source

