Pathophysiology, Treatment, and Prognosis of Thrombocytopenia, Anasarca, Fever, Reticulin Fibrosis/Renal Failure, and Organomegaly (TAFRO) Syndrome: A Review. [PDF]
Curr Issues Mol BiolTAFRO syndrome, first reported in 2010, is a systemic inflammatory disease with a rapid onset and potentially fatal course if not treated promptly and appropriately.
Kakutani T, Kamada R, Tamai Y.
europepmc +2 more sources
Case report: A case of acute exacerbation of interstitial pneumonia associated with TAFRO syndrome [PDF]
, 2023 Cytokine storm caused by the overproduction of inflammatory interleukin (IL)-6 plays a central role in the development of acute inflammation. The extremely rare disease, TAFRO syndrome, progresses quickly.
Eri Shishido +7 more
core +1 more source
TAFRO syndrome was effectively treated with an inexpensive novel scheme: A case report
Clinical Case Reports, Volume 11, Issue 2, February 2023., 2023 The combination of methylprednisolone and mycophenolate mofetil is effective for TAFRO syndrome. Abstract 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
Shan Meng +7 more
wiley +1 more source
A clinical, histological and transcriptomic characterization of a selected series of Castleman disease’s cases [PDF]
, 2023 Castleman disease (CD) is a rare lymphoproliferative disorder that includes various clinico-pathological subtypes. According to clinical course CD is divided in unicentric CD (UCD) and multicentric CD (MCD).
FRATICELLI, SARA
core
eJHaem, 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 multicentric Castleman disease in an adolescent diagnosed following COVID‐19 infection
, 2023 Pediatric Blood &Cancer, Volume 70, Issue 6, June 2023.
Eman Mosleh +5 more
wiley +1 more source
Lymphadenopathy in the rheumatology practice: a pragmatic approach [PDF]
, 2023 Lymphadenopathy is a common clinical finding and diagnostic challenge within general medicine and rheumatology practice. It may represent a primary manifestation of an underlying immune-mediated disease or indicate an infectious or neoplastic ...
Bongiovanni, Lucia +5 more
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TAFRO Syndrome in Caucasians: A Case Report and Review of the Literature
Frontiers in Medicine, 2017 BackgroundTAFRO syndrome has been reported in Japan among human herpesvirus 8 (HHV-8)-negative/idiopathic multicentric Castleman’s disease (iMCD) patients.
Céline Louis +8 more
doaj +1 more source
Spontaneous remission of iMCD-TAFRO: a case report
Annals of HematologyIdiopathic multicentric Castleman disease (iMCD)- TAFRO (thrombocytopenia, ascites, fever, reticulin fibrosis and organomegaly) is a clinically severe situation characterized by cytokine storms that are potentially fatal, necessitating prompt and decisive medical intervention.
Yuchong Qiu +4 more
openaire +2 more sources
Computed tomography findings of idiopathic multicentric Castleman disease subtypes [PDF]
This study retrospectively evaluated the computed tomography (CT) findings of idiopathic multicentric Castleman disease (iMCD) at a single center and compared the CT findings of iMCD-TAFRO with those of iMCD-non-TAFRO.
Asahara, Takashi +9 more
core +1 more source