Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Shouichi Okamoto"'
Autor:
Shouichi Okamoto, Mariko Shinomiya
Publikováno v:
Respiratory Medicine Case Reports, Vol 50, Iss , Pp 102056- (2024)
The cardiotoxicity of osimertinib, an epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor, has been recently reported when treating EGFR mutation-positive non-small cell lung cancer. In this report, we describe a case of an 81-year-old
Externí odkaz:
https://doaj.org/article/03ff8b859c684342ac48debeb868d16f
Autor:
Shouichi Okamoto, Kengo Koike, Mitsuaki Sekiya, Koichi Nishino, Tomoyasu Mimori, Kazuhisa Takahashi
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-6 (2022)
Abstract Background Lung involvement in inflammatory bowel diseases usually follows colitis. However, the time to lung involvement onset varies depending on the case, and pulmonary lesions are usually not parallel to exacerbations of the colitis. Cas
Externí odkaz:
https://doaj.org/article/4852b445ef794c7a9302a8bd5256bb22
Autor:
Naho Sakamoto, Motoyasu Kato, Toshihiko Ohni, Yuriko Terayama, Shun Nakazawa, Shouichi Okamoto, Jun Ito, Kazuhisa Takahashi
Publikováno v:
Respirology Case Reports, Vol 11, Iss 3, Pp n/a-n/a (2023)
Key message This is the first case confirmed the association between PI development and nintedanib by the reproducibility of PI development. In patients taking a combination treatment with corticosteroid and nintedanib, clinicians should be careful r
Externí odkaz:
https://doaj.org/article/ade989f429654e97aea378864091f4b2
Autor:
Shouichi Okamoto, Hiroki Ebana, Masatoshi Kurihara, Keiko Mitani, Etsuko Kobayashi, Takuo Hayashi, Yasuhito Sekimoto, Koichi Nishino, Mizuto Otsuji, Toshio Kumasaka, Kazuhisa Takahashi, Kuniaki Seyama
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Abstract Birt–Hogg–Dubé syndrome (BHDS), an autosomal dominant inheritance disease caused by folliculin (FLCN) mutations, is associated with lung cysts and spontaneous pneumothorax. The possibility of FLCN haploinsufficiency in pleural mesotheli
Externí odkaz:
https://doaj.org/article/cd2ed7a6da7f482eb03fc71e356f40e6
Autor:
Koichi Nishino, Yasuhiro Yoshimatsu, Tomoki Muramatsu, Yasuhito Sekimoto, Keiko Mitani, Etsuko Kobayashi, Shouichi Okamoto, Hiroki Ebana, Yoshinori Okada, Masatoshi Kurihara, Kenji Suzuki, Johji Inazawa, Kazuhisa Takahashi, Tetsuro Watabe, Kuniaki Seyama
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Lymphangioleiomyomatosis (LAM) is a rare pulmonary disease characterised by the proliferation of smooth muscle-like cells (LAM cells), and an abundance of lymphatic vessels in LAM lesions. Studies reported that vascular endothelial growth fa
Externí odkaz:
https://doaj.org/article/2ab2d6be5e714483911e6f086b4389fc
Autor:
Yasuhito Sekimoto, Kazuhiro Suzuki, Makiko Okura, Takuo Hayashi, Hiroki Ebana, Toshio Kumasaka, Keiko Mitani, Koichi Nishino, Shouichi Okamoto, Etsuko Kobayashi, Kazuhisa Takahashi, Kuniaki Seyama
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Lymphangioleiomyomatosis (LAM) is a rare destructive lung disease characterized by multiple thin-walled pulmonary cysts. The currently proposed diagnostic algorithm emphasizes the characteristic cystic appearance on high-resolution computed
Externí odkaz:
https://doaj.org/article/061298c7bdce432fb4472fcc89a17959
Autor:
Shouichi Okamoto, Kazuhiro Suzuki, Takuo Hayashi, Keiko Muraki, Tetsutaro Nagaoka, Koichi Nishino, Yasuhito Sekimoto, Shinichi Sasaki, Kazuhisa Takahashi, Kuniaki Seyama
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)
Abstract Background A guide of patient selection for establishing the diagnosis of lymphangioleiomyomatosis (LAM) by transbronchial lung biopsy (TBLB) has not been established, although the pathological confirmation of LAM by lung biopsy is desirable
Externí odkaz:
https://doaj.org/article/b0d113b9f35d4c16b83a0c1bdf4d88a4
Autor:
Shouichi Okamoto, Isao Kobayashi, Hiroshi Moriyama, Mayuka Tanimura, Kotaro Kadoya, Hiroki Ienaga, Toshiaki Kikuchi, Kazuhisa Takahashi
Publikováno v:
Respiratory Medicine Case Reports, Vol 37, Iss , Pp 101665- (2022)
Pleural disease in silicosis remains an underrecognized entity. Herein, we describe the case of an 85-year-old man with a 20-year history of silica exposure between the ages of 9–28 years. He presented with bilateral exudative pleural effusions, an
Externí odkaz:
https://doaj.org/article/b598387d9fc7454198e7b5ea1851cf7d
Publikováno v:
Respiratory Medicine Case Reports, Vol 33, Iss , Pp 101416- (2021)
Unsuspected, non-asphyxiating, aspirated foreign body often masquerades as unresolved pneumonia, bronchiolitis or bronchial asthma. We report herein an 82-year-old, male patient with pleural effusion. Although the patient received the diagnosis of he
Externí odkaz:
https://doaj.org/article/811a223b801e4bf192bf776333fcfcd1
Autor:
Teruaki Mizobuchi, Masatoshi Kurihara, Hiroki Ebana, Sumitaka Yamanaka, Hideyuki Kataoka, Shouichi Okamoto, Etsuko Kobayashi, Toshio Kumasaka, Kuniaki Seyama
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-7 (2018)
Abstract Background Birt-Hogg-Dubé syndrome (BHDS) is a recently recognized inherited multiple cystic lung disease causing recurrent pneumothoraces. Similarly to the lesions in patients with lymphangioleiomyomatosis (LAM), the pulmonary cysts are in
Externí odkaz:
https://doaj.org/article/c779dfb0e3a243929278ca8467f6eafd