Results 21 to 30 of about 1,018 (169)

TAFRO Syndrome: Guidance for Managing Patients Presenting Thrombocytopenia, Anasarca, Fever, Reticulin Fibrosis, Renal Insufficiency, and Organomegaly [PDF]

Biomedicines
TAFRO syndrome is an inflammatory disorder of unknown etiology characterized by thrombocytopenia, anasarca, fever, reticulin fibrosis, renal insufficiency, and organomegaly. Despite great advancements in research on the TAFRO syndrome in the last decade,
Katsuhiro Miura, Haruna Nishimaki-Watanabe, Hiromichi Takahashi, Masaru Nakagawa, Shimon Otake, Takashi Hamada, Takashi Koike, Kazuhide Iizuka, Yuuichi Takeuchi, Kazuya Kurihara, Toshihide Endo, Shun Ito, Hironao Nukariya, Takahiro Namiki, Yoshiyuki Hayashi, Hideki Nakamura   +15 more
doaj   +2 more sources

Pathophysiology, Treatment, and Prognosis of Thrombocytopenia, Anasarca, Fever, Reticulin Fibrosis/Renal Failure, and Organomegaly (TAFRO) Syndrome: A Review [PDF]

Current Issues in Molecular Biology
TAFRO syndrome, first reported in 2010, is a systemic inflammatory disease with a rapid onset and potentially fatal course if not treated promptly and appropriately.
Takuya Kakutani, Riko Kamada, Yotaro Tamai   +2 more
doaj   +2 more sources

Primary Sjögren’s Syndrome Accompanied by Clinical Features of TAFRO Syndrome [PDF]

Case Reports in Rheumatology, 2020
Sjögren’s syndrome (SS) is associated with not only sicca symptoms but also various symptoms caused by extraglandular manifestation. The pathophysiology and comorbidities of TAFRO syndrome (thrombocytopenia, anasarca, fever, reticulin fibrosis, and ...
Eiji Suzuki, Takuya Ichimura, Satoru Kimura, Takashi Kanno, Kiyoshi Migita   +4 more
doaj   +4 more sources

TAFRO syndrome is associated with anti-SSA/Ro60 antibodies, in contrast to idiopathic castleman disease [PDF]

Scientific Reports
TAFRO syndrome is an acute systemic inflammatory disease characterized by thrombocytopenia, anasarca, fever, reticulin fibrosis/renal dysfunction, and organomegaly.
Mirei Shirakashi, Yuri Nishida, Ran Nakashima, Masakazu Fujimoto, Ryosuke Hiwa, Hideaki Tsuji, Koji Kitagori, Shuji Akizuki, Akio Morinobu, Hajime Yoshifuji   +9 more
doaj   +2 more sources

TAFRO syndrome: New subtype of idiopathic multicentric Castleman disease [PDF]

Bosnian Journal of Basic Medical Sciences, 2017
Castleman disease (CD) describes a group of three rare and poorly understood lymphoproliferative disorders that have heterogeneous clinical symptoms and common lymph node histopathological features.
David C Fajgenbaum, Gordan Srkalovic, Inga Marijanovic, Maya B Srkalovic   +3 more
core   +5 more sources

Biomarkers and Signaling Pathways Implicated in the Pathogenesis of Idiopathic Multicentric Castleman Disease/Thrombocytopenia, Anasarca, Fever, Reticulin Fibrosis, Renal Insufficiency, and Organomegaly (TAFRO) Syndrome [PDF]

Biomedicines
Idiopathic multicentric Castleman disease (iMCD) and TAFRO syndrome present a variety of symptoms thought to be caused by excessive inflammatory cytokines and chemokines, but the underlying mechanisms are unknown.
Remi Sumiyoshi, Tomohiro Koga, Atsushi Kawakami   +2 more
doaj   +2 more sources

Severe coronavirus disease 2019 in a patient with TAFRO syndrome: A case report [PDF]

Clinical Infection in Practice, 2022
Background: TAFRO syndrome, a subtype of idiopathic multicentric Castleman disease, is an acute or subacute systemic inflammatory disease that causes fever, generalized oedema (pleural effusion or ascites), and thrombocytopenia and is associated with ...
Kengo Oshima, Hajime Kanamori, Kentarou Takei, Hiroaki Baba, Koichi Tokuda   +4 more
doaj   +2 more sources

Multicentric Castleman disease presenting with orbital involvement progressing to TAFRO syndrome: a case report [PDF]

BMC Ophthalmology
Background Castleman Disease (CD) can be unicentric or multicentric, with the ocular involvement rare; notably, the aggressive TAFRO syndrome (TS) is a subtype of idiopathic multicentric CD (iMCD). Ocular involvement in CD is rare, and to date, there are
Yuanfeng Wei, Jing Qi, Jiawei Yan, Guangjian Gao, Xinyue Ji, Danning Yu, Wanru Chen, Dongping Huang   +7 more
doaj   +2 more sources

Stepwise Treatment for TAFRO Syndrome. [PDF]

J Med Cases, 2023
TAFRO syndrome, a rapidly progressive and fatal disease, is rare, and its etiology remains unknown. It is characterized by thrombocytopenia, anasarca (edema, pleural effusion, and ascites), fever, reticulin fibrosis (or renal insufficiency), and organomegaly with Castleman disease (CD)-like histological features in the lymph nodes.
Ide M, Yokoyama T, Ishikawa M, Kojima K.
europepmc   +3 more sources

Radiological Imaging Findings of Adrenal Abnormalities in TAFRO Syndrome: A Systematic Review [PDF]

Biomedicines
This systematic review article aims to investigate the clinical and radiological imaging characteristics of adrenal abnormalities in patients with thrombocytopenia, anasarca, fever, reticulin fibrosis, renal dysfunction, and organomegaly (TAFRO) syndrome.
Ryo Kurokawa, Akira Baba, Rui Kano, Yo Kaneko, Mariko Kurokawa, Wataru Gonoi, Osamu Abe   +6 more
doaj   +2 more sources