Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Kazue, Takai"'
Autor:
Kazue Takai
Publikováno v:
Biomedicines, Vol 12, Iss 3, p 652 (2024)
TAFRO (thrombocytopenia, anasarca, fever, reticulin fibrosis of bone marrow/renal dysfunction, organomegaly) syndrome is a systemic inflammatory disorder of unknown etiology. It has been recognized as a subtype of idiopathic multicentric Castleman di
Externí odkaz:
https://doaj.org/article/ad43b07717e34b59a03dd4675bfa1c94
Autor:
Yasufumi Masaki, Yusuke Ueda, Hiroto Yanagisawa, Kotaro Arita, Tomoyuki Sakai, Kazunori Yamada, Shuichi Mizuta, Toshihiro Fukushima, Kazue Takai, Sadao Aoki, Hiroshi Kawabata
Publikováno v:
Internal Medicine. 62:27-32
TAFRO syndrome was first described in 2010, standing for thrombocytopenia, anasarca, fever, reticulin fibrosis and organomegaly. Because the lymph node histopathology of TAFRO syndrome mimics idiopathic multicentric Castleman disease (iMCD), some res
Publikováno v:
Annals of Hematology
Although Castleman disease was first described in 1956, this disease includes various conditions, including unicentric Castleman disease with hyaline vascular histology, human herpesvirus-8 (HHV-8) related multicentric Castleman disease, idiopathic m
Autor:
Tomoyuki Sakai, Hiroshi Kawabata, Momoko Nishikori, Hiroto Yanagisawa, Shino Fujimoto, Kenji Nara, Nozomu Kurose, Kazue Takai, Yasufumi Masaki, Shin Ohara, Norifumi Tsukamoto, Sohsuke Yamada, Sadao Aoki
Publikováno v:
International Journal of Hematology. 113:73-80
TAFRO syndrome is a systemic inflammatory disorder of unknown etiology characterized by thrombocytopenia, anasarca, fever, reticulin myelofibrosis, renal dysfunction, and organomegaly. Mortality in patients with this syndrome is high; however, an opt
Autor:
Takeharu Kotani, Noriko Iwaki, Shino Fujimoto, Nozomu Kurose, Ritsuro Suzuki, Mitsuhiro Kawano, Akikatsu Nakashima, Yasufumi Masaki, Hiroshi Kawabata, Sadao Aoki, Kazue Takai
Publikováno v:
Journal of Clinical and Experimental Hematopathology : JCEH
Castleman disease is a polyclonal lymphoproliferative disease which is clinically classified into unicentric (UCD) and multicentric (MCD). TAFRO syndrome is a relatively new concept that partly overlaps with MCD. Due to their rarity, their incidence
Autor:
Kazutaka Sunami, Katsuhiro Miura, Kazue Takai, Sadao Aoki, Tomoki Origuchi, Masao Hagihara, Kenji Nara, Hiroto Yanagisawa, Toshio Kitawaki, Shino Fujimoto, Yoshitaka Sunami, Hiroshi Yamamoto, Hiroshi Kawabata, Masanori Kobayashi, Taro Masunari, Masakuni Tanimizu, Keiko Yamagami, Chikako Kato, Tomoyuki Sakai, Yasufumi Masaki, Norifumi Tsukamoto, Nobuhiko Nakamura
Publikováno v:
International Journal of Hematology
To identify prognostic factors for TAFRO syndrome, a rare inflammatory disorder of unknown etiology characterized by thrombocytopenia, anasarca, fever, reticulin myelofibrosis, renal dysfunction, and organomegaly. Data of patients with TAFRO syndrome
Autor:
Tomoki Origuchi, Toshio Kitawaki, Kazue Takai, Hiroshi Kawabata, Masanori Kobayashi, Katsuhiro Miura, Yoshitaka Sunami, Hiroshi Yamamoto, Kazutaka Sunami, Keiko Yamagami, Shino Fujimoto, Tomoyuki Sakai, Chikako Kato, Nobuhiko Nakamura, Masao Hagihara, Norifumi Tsukamoto, Yasufumi Masaki, Sadao Aoki, Taro Masunari, Hiroto Yanagisawa, Masakuni Tanimizu, Kenji Nara
Publikováno v:
International Journal of Hematology. 114:301-302
Autor:
Shino, Fujimoto, Hiroshi, Kawabata, Tomoyuki, Sakai, Hiroto, Yanagisawa, Momoko, Nishikori, Kenji, Nara, Shin, Ohara, Norifumi, Tsukamoto, Nozomu, Kurose, Sohsuke, Yamada, Kazue, Takai, Sadao, Aoki, Yasufumi, Masaki
Publikováno v:
International journal of hematology. 113(1)
TAFRO syndrome is a systemic inflammatory disorder of unknown etiology characterized by thrombocytopenia, anasarca, fever, reticulin myelofibrosis, renal dysfunction, and organomegaly. Mortality in patients with this syndrome is high; however, an opt
Autor:
Katsuhiro Miura, Norifumi Tsukamoto, Sadao Aoki, Hiroshi Kawabata, Nozomu Kurose, Kazue Takai, Shigeo Nakamura, Yasuhito Ishigaki, Shino Fujimoto, Yasufumi Masaki
Publikováno v:
International journal of hematology. 111(1)
Autor:
Hiroshi Kawabata, Shino Fujimoto, Akihiro Shioya, Shigeo Nakamura, Kazue Takai, Xin Guo, Nozomu Kurose, Yasufumi Masaki, Kenichi Mizutani, Motona Kumagai, Sohsuke Yamada, Sadao Aoki
Publikováno v:
Pathology, research and practice. 215(10)
Idiopathic multicentric Castleman disease (iMCD) is a systemic inflammatory disease of unknown etiology caused by hypercytokinemia. Recently, TAFRO ( t hrombocytopenia, a nasarca, f ever, r enal failure or r eticulin fibrosis, and o rganomegaly) synd