Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Masaru Furumoto"'
Publikováno v:
iGIE.
Publikováno v:
Internal medicine (Tokyo, Japan).
Autor:
Masayuki Sakae, Hideki Tsukazaki, Takeo Yasuda, Yukari Sakae, Takashi Tsukazaki, Atsushi Ishihara, Masaru Furumoto, Tooru Hamada
Publikováno v:
International Journal of Surgery Case Reports
Highlights • Mammary-type Myofibroblastoma of the Inguinal Region is very rare. • Prognosis of this disease is good after surgical resection. • The correct diagnosis and treatment is important. • We think that it is useful to share knowledge
Autor:
Kentaro Inoue, Masayuki Sakae, Tooru Hamada, Yukari Sakae, Masaru Furumoto, Takeo Yasuda, Takashi Tsukazaki
Publikováno v:
Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association). 78:1978-1982
Publikováno v:
Internal Medicine; 2023, Vol. 62 Issue 15, p2289-2290, 2p
Autor:
Tetsuya Miyamaoto, Yoshiki Tohma, Akira Takahashi, Nobuhiko Mukohara, Keitarou Nakagiri, Masaru Furumoto, Junya Sato
Publikováno v:
Nihon Kyukyu Igakukai Zasshi. 22:181-187
Autor:
Ayumi Sei, Naoki Tsujimoto, Mihoko Furumoto, Masato Kinugasa, Yoshihiko Miyazaki, Toshiyo Nakagawa, Masaru Furumoto, Masamichi Sasaki
Publikováno v:
The Journal of the Japanese Society of Clinical Cytology. 42:131-136
背景:子宮頸部の紡錘形細胞癌は非角化型扁平上皮癌のまれな一亜型である. 今回, その1例について報告し, 文献的考察を加える.症例:42歳経産婦, 褐色帯下を主訴として受診, 子宮頸部に限
Autor:
Masaru Furumoto, Yoshito Tsukazaki, Yoshikazu Fukuda, Satoru Hirao, Hiroaki Kinoshita, Hiroshi Takatori, Yukio Yoshioka
Publikováno v:
The journal of the Japanese Practical Surgeon Society. 55:2325-2330
Leiomyosarcoma arising from the residual stomach is extremely rare. This paper describes a case of this tumor resected at the hospital with an analysis of 22 cases seen in the Japanese literature. A 78-year-old female was transferred by an ambulance
Autor:
Masaru Furumoto, Kyoichi Ogawa, Shigeki Nishimoto, Sachiko Futami, Shinichirou Matsumoto, Rieko Minami, Keisuke Inoue, Tomio Yamasaki, Kohji Matsuba, Tatsurou Asada
Publikováno v:
Internal Medicine. 32:257-260
A case of malignant thymoma presenting as the superior vena cava syndrome is reported. A 56-year old male was admitted with superior vena cava syndrome. CT and NMR-CT scan showed a solid homogenous superior mediastinal mass; which filled the lumen of
Autor:
Kohji, Maeda, Yasushi, Kita, Satoshi, Uehara, Osamu, Yamasaki, Mitsue, Rikimaru, Naoki, Saji, Masayasu, Tabuti, Masaru, Furumoto
Publikováno v:
No to shinkei = Brain and nerve. 58(7)
We reported a 60-year-old woman who suffered from isolated neurosarcodosis. She was presenting comprehensive dysfunction and intermittent high fever. In several months she gradually developed dysorientation, amnesia, dementia. However, no focal sign