Results 41 to 50 of about 1,018 (169)

Idiopathic multicentric Castleman disease: a mysterious case of generalized lymphadenopathy [PDF]

open access: yes, 2023
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]

open access: yesIntern Med
Kobayashi T   +12 more
europepmc   +3 more sources

Borderline Case of TAFRO Syndrome and POEMS Syndrome

open access: yesInternal Medicine, 2021
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

open access: yesKidney Medicine, 2021
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]

open access: yes, 2021
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

Global public awareness of Castleman disease and TAFRO syndrome between 2015 and 2021: A Google Trends analysis

open access: yeseJHaem, 2022
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]

open access: yes, 2022
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]

open access: yesInt J Hematol, 2023
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

open access: yesBMC Nephrology, 2022
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

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