Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Yuma Nato"'
Publikováno v:
Clinical Case Reports, Vol 12, Iss 5, Pp n/a-n/a (2024)
Key Clinical Message This case of non‐nodal mantle cell lymphoma (MCL) showcases atypical hairy cell‐like features, distinguishing it via next‐generation sequencing. Despite a TP53 mutation indicating poor prognosis, our case followed an indole
Externí odkaz:
https://doaj.org/article/799d6fb4f7e9442db2afedbd82e6afa7
Autor:
Yuma Nato, Keiki Nagaharu, Keika Itoh, Naoki Shinke, Keiko Maeyama, Akihiko Sawaki, Hiroyuki Miyashita
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2024 (2024)
Background. Autoimmune hemolytic anemia (AIHA) associated with solid tumors such as mature cystic teratomas is rare and poorly understood. Here, we report a successfully treated case of secondary AIHA in a mature cystic teratoma containing antibodies
Externí odkaz:
https://doaj.org/article/9e34c7ee82df41fdac934ca49576d80c
Autor:
Yuki Kageyama, Kenshiro Tsuda, Yuma Nato, Keiki Nagaharu, Kazutaka Suzuki, Akihiko Sawaki, Hiroyuki Miyashita
Publikováno v:
Case Reports in Hematology, Vol 2021 (2021)
Sézary syndrome is a rare leukemic type of cutaneous T-cell lymphoma characterized by the presence of neoplastic T cells with cerebriform nuclei (Sézary cells) in the skin, lymph nodes, and peripheral blood. Typical Sézary cells have a CD3+CD4+CD8
Externí odkaz:
https://doaj.org/article/c3dae780e75c4b1eb909165741a1f287
Autor:
Yuma Nato, Yuki Kageyama, Kazutaka Suzuki, Keiko Shimojima Yamamoto, Hitoshi Kanno, Hiroyuki Miyashita
Publikováno v:
Internal Medicine. 62:107-111
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50c77f7722e0ee43c44d8f5ea83ad77e
https://doi.org/10.2169/internalmedicine.9478-22
https://doi.org/10.2169/internalmedicine.9478-22
Autor:
Yuma Nato, Keiki Nagaharu, Kanako Inoue, Kodai Yabu, Akihiko Sawaki, Takuya Shiotani, Yuki Kageyama, Ken Tanaka, Koichi Ohshima, Hiroyuki Miyashita
Publikováno v:
Journal of Clinical and Experimental Hematopathology. 62:238-241
Richter's syndrome (RS) of the central nervous system (CNS) is known to have an extremely poor prognosis. Ibrutinib has been reported to have some activity in patients with RS, despite its poor prognosis. Although ibrutinib crosses the blood-brain ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eb924d78d09e71f736b354f8c8b4ff1
https://doi.org/10.3960/jslrt.22017
https://doi.org/10.3960/jslrt.22017
Autor:
Yuma, Nato, Yuki, Kageyama, Kazutaka, Suzuki, Keiko, Shimojima Yamamoto, Hitoshi, Kanno, Hiroyuki, Miyashita
Publikováno v:
Internal medicine (Tokyo, Japan). 62(1)
Most patients with hereditary spherocytosis (HS) have a family history of disease, while those without such a history are difficult to diagnose. We herein report a case of HS with no family history harboring a novel heterozygous mutation of SPTA1, c.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::12774a8386e25dcefd4435fac748bfa1
https://pubmed.ncbi.nlm.nih.gov/35650129
https://pubmed.ncbi.nlm.nih.gov/35650129
Autor:
Isao Tawara, Eri Nakano, Atsushi Fujieda, Yuma Nato, Kazuko Ino, Yuki Kageyama, Hiroshi Imai, Motoko Yamaguchi, Kyosuke Tanaka, Kana Miyazaki, Takeshi Matsumoto, Naoyuki Katayama
Publikováno v:
International Journal of Hematology. 114:129-135
Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL) is a rare subtype of intestinal T-cell lymphoma that occurs mostly in Asia. CHOP-like therapy is usually selected, but the prognosis is very poor. This report concerns a 43-year-old woman
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::939ad3660d5cd594af490493b38f11a9
https://doi.org/10.1007/s12185-021-03107-9
https://doi.org/10.1007/s12185-021-03107-9
Autor:
Yuma, Nato, Yuki, Kageyama, Kazutaka, Suzuki, Akihiko, Sawaki, Takuya, Shiotani, Shuji, Yamamoto, Hiroyuki, Miyashita
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 63(1)
At initial diagnosis, central nervous system (CNS) involvement in acute promyelocytic leukemia (APL) is rare. Here, we report a case of newly diagnosed APL with CNS involvement that was successfully treated with all-trans retinoic acid (ATRA)-combine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8fe6177c0e081f395bc2751da2ce9cd5
https://pubmed.ncbi.nlm.nih.gov/35135948
https://pubmed.ncbi.nlm.nih.gov/35135948
Autor:
Yuma Nato, Kana Miyazaki, Hiroshi Imai, Eri Nakano, Yuki Kageyama, Kazuko Ino, Atsushi Fujieda, Takeshi Matsumoto, Isao Tawara, Kyosuke Tanaka, Motoko Yamaguchi, Naoyuki Katayama
Publikováno v:
International Journal of Hematology. 115:452-453
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0f306acb682ed3a0964968976f4a3b6
https://doi.org/10.1007/s12185-022-03295-y
https://doi.org/10.1007/s12185-022-03295-y
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 62(3)
Acquired thrombotic thrombocytopenic purpura (aTTP) is a life-threatening systemic thrombotic microangiopathy characterized by the presence of anti-ADAMTS13 antibodies (inhibitor). Here we report the case of a patient with refractory aTTP successfull
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4ec00738abae0d52b24d66db9081ab95
https://pubmed.ncbi.nlm.nih.gov/33828010
https://pubmed.ncbi.nlm.nih.gov/33828010