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Published in 2022 at "Hematological oncology"
DOI: 10.1002/hon.3075
Abstract: TAFRO syndrome (thrombocytopenia, anasarca, fever, reticulin fibrosis/renal failure, and organomegaly) is rare in clinical practice. It is a systemic inflammatory disease caused by a cytokine storm. Its clinical manifestations include thrombocytopenia, systemic edema, fever, bone…
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Keywords:
tafro syndrome;
known half;
disease;
syndrome disease ... See more keywords
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Published in 2019 at "International Journal of Hematology"
DOI: 10.1007/s12185-019-02604-2
Abstract: TAFRO syndrome and acquired hemophilia A (AHA) are rare, life-threatening diseases; however, the relationship between these two diseases is unknown. A 25-year-old man was transferred to our hospital because of bleeding tendency accompanied by multiple…
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Keywords:
features tafro;
acquired hemophilia;
cardiopulmonary arrest;
tafro syndrome ... See more keywords
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Published in 2018 at "Human pathology"
DOI: 10.1016/j.humpath.2018.03.021
Abstract: An 84-year-old Japanese man was admitted due to anasarca, thrombocytopenia, systemic inflammation, and progressive renal insufficiency, resistance to diuretics, glucocorticoid therapy, and plasma exchange. Renal biopsy showed diffuse endocapillary proliferation and mesangiolysis without any immune…
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Keywords:
thrombocytopenia;
histology;
histology patient;
renal histology ... See more keywords
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Published in 2019 at "Modern Rheumatology"
DOI: 10.1080/14397595.2016.1206243
Abstract: Abstract We report a case of a 46-year-old woman with fever, pleural effusion, massive ascites, severe edema, hepatosplenomegaly, elevation of serum creatinine level, proteinuria, and severe thrombocytopenia. Her clinical features were compatible with TAFRO syndrome…
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Keywords:
case;
castleman disease;
variant multicentric;
multicentric castleman ... See more keywords
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Published in 2018 at "Medicine"
DOI: 10.1097/md.0000000000011045
Abstract: Rationale: TAFRO syndrome is a systemic inflammatory disorder characterized by thrombocytopenia, anasarca, fever, reticulin fibrosis, renal dysfunction, and organomegaly. In contrast to that in multicentric Castleman disease, interleukin-6 targeting strategies seem ineffective in some TAFRO…
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Keywords:
treatment;
case;
tacrolimus;
tafro syndrome ... See more keywords
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Published in 2022 at "Medicine"
DOI: 10.1097/md.0000000000032200
Abstract: Rationale: Thrombocytopenia, anasarca, fever, reticulin fibrosis, renal dysfunction, and organomegaly (TAFRO) syndrome are nonmalignant but life-threatening systemic inflammatory disorders. However, many patients are refractory to treatment, resulting in significant morbidity and mortality. Additionally, established treatment…
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Keywords:
tafro syndrome;
thrombocytopenia anasarca;
treatment resistant;
anasarca fever ... See more keywords
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Published in 2020 at "European Journal of Haematology"
DOI: 10.1111/ejh.13473
Abstract: Thrombocytopenia, Anasarca, reticulin Fibrosis of the bone marrow, Renal dysfunction and organomegaly (TAFRO) syndrome is a very rare and severe variant of multicenter Castleman's disease firstly reported in Japan in 2010.1,2 TAFRO syndrome is a…
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Keywords:
frontline siltuximab;
siltuximab rituximab;
rituximab tafro;
tafro syndrome ... See more keywords
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Published in 2020 at "BMJ Case Reports"
DOI: 10.1136/bcr-2019-234155
Abstract: TAFRO (thrombocytopenia, anasarca, fever, reticulin myelofibrosis or renal dysfunction and organomegaly) syndrome is a systemic inflammatory disease characterised by thrombocytopenia, anasarca, fever or inflammatory syndrome, reticulin myelofibrosis or renal dysfunction and organomegaly. It was first…
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Keywords:
hypothyroidism;
thrombocytopenia;
fever;
tafro syndrome ... See more keywords
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Published in 2019 at "BMC Nephrology"
DOI: 10.1186/s12882-019-1574-9
Abstract: BackgroundTAFRO syndrome is a systemic inflammatory disorder that manifests as thrombocytopenia (T), anasarca (A), fever (F), reticulin fibrosis (R), and organomegaly (O). Renal dysfunction is frequently complicated with TAFRO syndrome, however, it is challenging to…
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Keywords:
biopsy;
case;
review;
glomerular microangiopathy ... See more keywords
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Published in 2019 at "Nagoya Journal of Medical Science"
DOI: 10.18999/nagjms.81.3.519
Abstract: ABSTRACT TAFRO syndrome is a novel disease concept characterized by Thrombocytopenia, Anasarca, myeloFibrosis, Renal dysfunction, Organomegaly, multiple lymphadenopathy and a histopathological pattern of atypical Castleman’s disease. A 58-year-old man was diagnosed as TAFRO syndrome by…
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Keywords:
thrombocytopenia anasarca;
fatal case;
treatment;
case ... See more keywords
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Published in 2022 at "Internal medicine"
DOI: 10.2169/internalmedicine.0267-22
Abstract: TAFRO syndrome, a rare systemic inflammatory disorder, commonly develops in an acute or subacute manner, with an aggressive clinical behavior. A substantial number of cases of TAFRO syndrome presenting with abdominal pain, and adrenal abnormalities…
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Keywords:
tafro syndrome;
adrenal swelling;
acute abdomen;
abdominal pain ... See more keywords