Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Yuji Yufu"'
Autor:
Yu Yagi, Eriko Nakashima, Motohiko Ikeda, Yoshimichi Tachikawa, Eriko Fujioka, Takamitsu Matsushima, Hayato Utsunomiya, Youko Suehiro, Tatsuro Goto, Akiko Takamatsu, Hiroshi Takatsuki, Hirofumi Ohno, Taisuke Narazaki, Hiroki Muta, Makoto Oyama, Akie Hirata, Mariko Tsuda, Mitsuo Kozuru, Yuji Yufu, Ilseung Choi, Naokuni Uike, Emi Tanaka, Shojiro Haji, Kaname Miyashita, Junichi Kiyasu, Yasuhiro Tsukamoto, Yasuhiro Nakashima
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 20:e445-e453
Background We retrospectively analyzed patients with untreated aggressive adult T-cell leukemia/lymphoma who received the modified EPOCH (mEPOCH) regimen. Patients and Methods Patients received up to 6 mEPOCH cycles. Etoposide (50 mg/m2/day), doxorub
Autor:
Motoaki Shiratsuchi, Hiroki Muta, Mariko Tsuda, Junichi Kiyasu, Yoshihiro Ogawa, Kouichi Ohshima, Fumiko Arakawa, Yuji Yufu, Shojiro Haji, Motohiko Ikeda, Takamitsu Matsushima, Hiroaki Miyoshi, Yoshimichi Tachikawa, Yasuhiro Tsukamoto
Publikováno v:
Pathology International. 68:485-490
Although gamma heavy chain disease (γ-HCD) lesions occasionally morphologically resemble angioimmunoblastic T-cell lymphoma (AITL), no association has been described in detail due to the rarity of the disease. In this report, we present a rare manif
Autor:
Mariko Tsuda, Yoshihiro Ogawa, Motoaki Shiratsuchi, Yuji Yufu, Yasuhiro Tsukamoto, Motohiko Ikeda, Junichi Kiyasu
Publikováno v:
Internal Medicine
A 73-year-old man with primary myelofibrosis (PMF) was being treated with hydroxyurea, which was changed to ruxolitinib treatment because of worsening constitutional symptoms. Although ruxolitinib rapidly induced relief, he developed a high-grade fev
Autor:
Junichi, Kiyasu, Fumiko, Arakawa, Shojiro, Haji, Yoshimichi, Tachikawa, Mariko, Tsuda, Yasuhiro, Tsukamoto, Motohiko, Ikeda, Hiroki, Muta, Takamitsu, Matsushima, Hiroaki, Miyoshi, Motoaki, Shiratsuchi, Yoshihiro, Ogawa, Kouichi, Ohshima, Yuji, Yufu
Publikováno v:
Pathology international.
Although gamma heavy chain disease (γ-HCD) lesions occasionally morphologically resemble angioimmunoblastic T-cell lymphoma (AITL), no association has been described in detail due to the rarity of the disease. In this report, we present a rare manif
Autor:
Ryoichi Takayanagi, Eriko Fujioka, Motoaki Shiratsuchi, Yuji Yufu, Yasuhiro Nakashima, Takamitsu Matsushima, Eriko Nakashima
Publikováno v:
Journal of Hematopoietic Cell Transplantation. 2:112-115
Autor:
Shojiro, Haji, Junichi, Kiyasu, Yoshimichi, Tachikawa, Jiro, Toyonaga, Motohiko, Ikeda, Mariko, Tsuda, Yasuhiro, Tsukamoto, Mitsuo, Kozuru, Yuji, Yufu
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 57(6)
Light-chain deposition disease (LCDD) is a rare plasma cell neoplasm that secretes an abnormal immunoglobulin light chain, which is deposited in tissues, leading to organ dysfunction. Spontaneous splenic rupture is a rare and life-threatening complic
Autor:
Motoaki Shiratsuchi, Koichi Ohshima, Koichi Akashi, Fumiko Arakawa, Daisuke Niino, Akie Hirata, Ayako Ichikawa, Ryoichi Takayanagi, Takashi Okamura, Yasunobu Abe, Ilseung Choi, Koji Nagafuji, Yasuo Sugita, Yuji Yufu, Junichi Kiyasu, Hiroaki Miyoshi, Naokuni Uike
Publikováno v:
Blood. 126(19)
Programmed cell death ligand 1 (PD-L1) is expressed on both select diffuse large B-cell lymphoma (DLBCL) tumor cells and on tumor-infiltrating nonmalignant cells. The programmed cell death 1 (PD-1)/PD-L1 pathway inhibits host antitumor responses; how
Autor:
Yuji Yufu, Junji Nishimura, Koichiro Muta, Satoshi Shiokawa, Nobuhisa Hirase, Hajime Nawata, Yasunobu Abe
Publikováno v:
Cancer Genetics and Cytogenetics. 117:113-117
These are the first cases of primary macroglobulinemia (PMG) with t(11;18)(q21;q21) reported in the literature. The first case was a 77-year-old man with macroglobulinemia (serum IgM: 8.36 g/dL). Abnormal lymphoid cells were detected in the blood and
Autor:
Ilseung Choi, Toshiyasu Taniguchi, Naokuni Uike, Toru Motokura, Koichi Ohshima, Shigeo Nakamura, Tatsuro Goto, Yasushi Yatabe, Mitsuo Kozuru, Yuji Yufu
Publikováno v:
ResearcherID
BACKGROUND The t(11;14)(q13;q32) translocation with cyclin D1 overexpression commonly is found in multiple myeloma (MM) and in mantle cell lymphoma (MCL). Several reports have shown that p53 mutations in MCL lead to blastoid transformation and a wors
Autor:
Mari Kannagi, Hiroyoshi Hattori, Ryuji Tanosaki, Yoshio Saburi, Mine Harada, Naokuni Uike, Jun Okamura, Masato Masuda, Atae Utsunomiya, Masao Tomonaga, Nobuhiro Kimura, Fumio Kawano, Yuji Yufu, Hiroshi Kikuchi, Shunro Sonoda
Publikováno v:
Blood. 105:4143-4145
Sixteen patients with adult T-cell leukemia/lymphoma (ATL) who were all over 50 years of age underwent allogeneic stem cell transplantation with reduced-conditioning intensity (RIST) from HLA-matched sibling donors after a conditioning regimen consis