Results 11 to 20 of about 1,018 (169)

Case report: Atypical POEMS syndrome without polyneuropathy, complicated by borderline TAFRO syndrome. [PDF]

open access: yesFront Med (Lausanne)
POEMS syndrome is a complex and rare hematological disease involving multiple physiological systems. According to the currently accepted diagnostic criteria for POEMS syndrome, polyneuropathy is one of the primary mandatory criteria.
Tan S   +8 more
europepmc   +6 more sources

TAFRO Syndrome [PDF]

open access: yesBalkan Medical Journal, 2020
Hirohisa Fujikawa, Makoto Araki
doaj   +4 more sources

Disseminated Mycobacterium genavense infection mimicking TAFRO syndrome [PDF]

open access: yesJournal of Infection and Chemotherapy, 2020
TAFRO syndrome is a rare variant of idiopathic multicentric Castleman's disease, for which disseminated non-tuberculous mycobacteria (NTM) infection must be excluded.
Fujimori, Takumi   +8 more
core   +5 more sources

TAFRO syndrome presenting as intrahepatic cholangitis on autopsy [PDF]

open access: yesClinical Case Reports, 2021
Elevation of ALP is an abnormal feature in TAFRO syndrome, but the cause is unknown. This article is the first report that histologically showed intrahepatic cholangitis may be the cause of ALP elevation in TAFRO syndrome.
Hiroaki Nishioka   +3 more
doaj   +4 more sources

Investigation of the Effect of Therapeutic Plasma Exchange for TAFRO Syndrome: A Pilot Study [PDF]

open access: yesBiomedicines
TAFRO syndrome is a rare systemic inflammatory disorder with a fatal course. Nevertheless, a definitive treatment strategy has not yet been established. Anti-inflammatory therapies, including glucocorticoid treatment and immunosuppressants, have not been
Kosuke Sonoda   +4 more
doaj   +2 more sources

Case report: A case of acute exacerbation of interstitial pneumonia associated with TAFRO syndrome. [PDF]

open access: yesFront Med (Lausanne), 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.
Shimada Y   +7 more
europepmc   +3 more sources

A Case of TAFRO Syndrome Developed after COVID-19 Vaccination [PDF]

open access: yesCase Reports in Nephrology, 2023
TAFRO syndrome is a systemic inflammatory disorder, which is characterized by thrombocytopenia, anasarca, fever, reticulin myelofibrosis, renal dysfunction, and organomegaly. It often presents with progressive clinical symptoms and can be fatal. COVID-19
Hitomi Hirose   +7 more
doaj   +2 more sources

A case of TAFRO syndrome with DIC and neurologic and cardiac involvement [PDF]

open access: yesClinical Case Reports, 2023
Key Clinical Message We highlight a novel case of TAFRO syndrome with disseminated intravascular coagulation, neurologic changes, and non‐ischemic cardiomyopathy.
Lindsay N. Moy   +4 more
doaj   +2 more sources

TAFRO syndrome was effectively treated with an inexpensive novel scheme: A case report [PDF]

open access: yesClinical Case Reports, 2023
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,
Shan Meng   +7 more
doaj   +2 more sources

TAFRO syndrome with abdominal pain as the first symptom accompanied by liver damage with hyperbilirubinemia: A case report [PDF]

open access: yesHeliyon
Thrombocytopenia, anasarca, fever, reticulin fibrosis on bone marrow biopsy/renal dysfunction, and organomegaly (TAFRO) syndrome are infrequent conditions with diverse clinical and pathological characteristics related to multi-organ damage. There are few
Yu Liu   +8 more
doaj   +2 more sources

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