Results 141 to 150 of about 1,018 (169)

Internal Medicine (2) [PDF]

, 2017
上野 博志, 傍島 光男, 坂本 有, 城宝 秀司, 小池 勤, 平井 忠和, 福田 信之, 絹川 弘一郎, 西田 邦洋, 野手 姫代美   +9 more
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Disseminated Mycobacterium genavense infection mimicking TAFRO syndrome

Disseminated Mycobacterium genavense infection mimicking TAFRO syndrome
TAFRO syndrome is a rare variant of idiopathic multicentric Castleman's disease, for which disseminated non-tuberculous mycobacteria (NTM) infection must be excluded. However, due to the slow and fastidious growth of the organisms, identification of the pathogen is often challenging.
openaire  

Recurrent Cerebral Hemorrhaging with Platelet Dysfunction Accompanied by Anti-glycoprotein VI Autoantibodies in a Patient with TAFRO Syndrome. [PDF]

Intern Med
Yamamoto A, Nishimori H, Shirai T, Takano K, Komura A, Kambara Y, Fukumi T, Urata T, Asada N, Ennishi D, Fujii K, Fujii N, Matsuoka KI, Niiya K, Suzuki-Inoue K, Maeda Y.   +15 more
europepmc   +1 more source

Long-term clinicopathological characteristics of TAFRO syndrome and its relapse: a case series study. [PDF]

Clin Kidney J
Yoshimura Y, Mizuno H, Ikuma D, Yamanouchi M, Sekine A, Suwabe T, Oba Y, Kurihara S, Sugimoto H, Inoue N, Yoshimoto M, Tanimizu H, Tsunoda S, Iijima M, Kono K, Kinowaki K, Ohashi K, Takazawa Y, Hasegawa E, Ubara Y, Sawa N.   +20 more
europepmc   +1 more source

Idiopathic Multicentric Castleman Disease With Thrombocytopenia, Anasarca, Fever, Reticulin Fibrosis/Renal Insufficiency, and Organomegaly (TAFRO) Syndrome in a Liver Transplant Recipient. [PDF]

ACG Case Rep J
Mashal FA, Awad JA, Tillman BF, Mosse CA, Thandassery RB.   +4 more
europepmc   +1 more source

腎臓高血圧内科学講座 [PDF]

, 2020

core  

A Case of Thrombocytopenia, Anasarca (Edema, Pleural Effusion, and Ascites), Fever, Reticulin Fibrosis/Renal Dysfunction, and Organomegaly (TAFRO) Syndrome Initially Not Presenting With Thrombocytopenia: A Role of Immature Platelet Fraction. [PDF]

Cureus
Kanda M, Kitamura K, Saito A, Hayashi K, Suzuki T.   +4 more
europepmc   +1 more source

Update and new approaches in the treatment of Castleman disease [PDF]

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TAFRO Syndrome

Hematology/Oncology Clinics of North America, 2018
TAFRO syndrome is a newly recognized variant of idiopathic multicentric Castleman disease (iMCD) that involves a constellation of syndromes: thrombocytopenia (T), anasarca (A), fever (F), reticulin fibrosis (R), and organomegaly (O). Thrombocytopenia and severe anasarca accompanied by relatively low serum immunoglobulin levels are characteristic ...
Takuro, Igawa, Yasuharu, Sato
openaire   +2 more sources

Glomeruloid hemangioma associated with TAFRO syndrome

Human Pathology, 2018
Glomeruloid hemangioma is a rare cutaneous lesion that has been considered as a specific cutaneous marker of POEMS syndrome. Herein, we present the first case of glomeruloid hemangioma associated with TAFRO syndrome, a unique variant of idiopathic multicentric Castleman disease.
Aya, Shinozaki-Ushiku, Takaaki, Higashihara, Masako, Ikemura, Junichiro, Sato, Masaomi, Nangaku, Tetsuo, Ushiku, Masashi, Fukayama   +6 more
openaire   +2 more sources