Results 151 to 160 of about 1,018 (169)
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[Clinical Anslysis of TAFRO Syndrome].
Zhongguo shi yan xue ye xue za zhi, 2023To investigate the clinical characteristics, diagnosis, and treatment of one patient with TAFRO syndrome, and to strengthen the understanding of this rare type.The clinical manifestations, diagnosis and treatment process, and prognosis of the patient admitted in Gansu Provincial People's Hospital were retrospectively analyzed.Combined with laboratory ...
Fei, Liu +6 more
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FDG PET/CT Findings in TAFRO Syndrome
Clinical Nuclear Medicine, 2018Abstract A 67-year-old woman with prolonged fever, thrombocytopenia, and renal dysfunction underwent FDG PET/CT to evaluate underlying causes, including malignancy. PET/CT showed FDG uptake in ascites, subcutaneous edema, lymph nodes, spleen, and bone marrow.
Masatoshi, Hotta +4 more
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TAFRO syndrome: A disease that known is half cured
Hematological Oncology, 2022Abstract Thrombocytopenia, anasarca, fever, reticulin fibrosis/renal failure, and organomegaly (TAFRO) syndrome 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 marrow fibrosis, renal insufficiency, and ...
Tingting Chen +3 more
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The experience of diagnosis and treatment for TAFRO syndrome
Annals of Hematology, 2023Early identification, diagnosis and treatment of TAFRO syndrome are very importants. We retrospectively analysed 6 patients with TAFRO syndrome. Their clinical manifestations, treatment methods, survival and other aspects were summarized. All patients were pathologically diagnosed with Castleman's disease, with fever, an inflammatory storm state and ...
Xiaolong Wu +9 more
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[A case report of TAFRO syndrome].
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences, 2021The study is to improve clinicians' understanding of TAFRO syndrome, to explore the diagnosis and treatment of TAFRO syndrome and to identify TAFRO syndrome in the early stage. The clinical manifestations, laboratory examination results, imaging manifestations, diagnosis and treatment of TAFRO syndrome were reported, and the literature of TAFRO ...
G P, Zhou, Q Y, Zhou, J H, Zhu
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[TAFRO syndrome and cutaneous necrotizing vasculitis].
La Revue de medecine interne, 2021TAFRO syndrome is a systemic inflammatory syndrome in the spectrum of Castleman's disease, associating thrombocytopenia, anasarca, fever, renal failure and/or reticulin myelofibrosis and organomegaly. Its association with necrotizing cutaneous vasculitis has not yet been reported.A 69-year-old woman presented with weight loss, fever, anasarca ...
J, Maquet +11 more
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Une anasarque fébrile révélant un syndrome TAFRO
La Revue de Médecine Interne, 2017Introduction Le syndrome TAFRO a ete decrit en 2010 comme une forme particuliere de maladie de castleman multicentrique associant une thrombopenie (T), une anasarque (A), une myelofibrose reticulinique (F), une insuffisance renale (R) et une organomegalie (O) [1] . Nous rapportons un cas d’anasarque febrile revelant ce syndrome.
F. Coutier +8 more
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Renal involvement in TAFRO syndrome: a review
Clinical and Experimental NephrologyRenal involvement in TAFRO syndrome is characterized clinically by general edema with ascites and pleural effusions and a rapidly progressive decline in renal function, with urinary protein levels of usually less than 1 g/day. The histologic features of the kidneys can be described as glomerular microangiopathy characterized by mesangiolysis or ...
Yoshifumi, Ubara, Naoki, Sawa
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Magnetic resonance imaging of bone marrow for TAFRO syndrome
Modern Rheumatology, 2016We report two cases of TAFRO syndrome, which is characterized by thrombocytopenia, anasarca, fever, renal insufficiency, and organomegaly. Magnetic resonance imaging (MRI) of the spine showed a dark medullary pattern in the bone marrow on the T1- and T2-weighted images of both patients. One patient showed complete resolution after treatment.
Gen, Nakamura +7 more
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TAFRO syndrome: 2 cases and review of the literature
Modern Rheumatology, 2015Recently, more than ten cases of thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly (TAFRO) syndrome or Castleman-Kojima disease exhibiting such symptoms as thrombocytopenia, anasarca, fever, reticulin fibrosis and organomegaly have been reported in Japan. We have found two cases of TAFRO syndrome and have reviewed another eighteen
Mikako, Kawashima +11 more
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