Zobrazeno 1 - 10
of 732
pro vyhledávání: '"Hideyuki ISHIDA"'
Autor:
Nobuhiko Kanaya, Thijs A. vanSchaik, Hideki Aoki, Yumiko Sato, Fumitaka Taniguchi, Kunitoshi Shigeyasu, Kokichi Sugano, Kiwamu Akagi, Hideyuki Ishida, Kohji Tanakaya
Publikováno v:
Annals of Gastroenterological Surgery, Vol 8, Iss 6, Pp 1008-1016 (2024)
Abstract Aim Lynch syndrome (LS) is a dominantly inherited syndrome characterized by an increased risk for LS associated tumors such as colorectal cancer (CRC) and gastric cancer (GC). However, the clinical benefit of surveillance for GC remains uncl
Externí odkaz:
https://doaj.org/article/e1676b30cca14d9bbabe786e88822a90
Autor:
Yoshiko Mori, Okihide Suzuki, Noriko Tanabe, Aoi Sugino, Takehiro Shiraishi, Norimichi Chiyonobu, Kenichi Chikatani, Noriyasu Chika, Satoshi Hatano, Takatoshi Matsuyama, Keiichiro Ishibashi, Hideyuki Ishida
Publikováno v:
Journal of the Anus, Rectum and Colon, Vol 8, Iss 4, Pp 289-297 (2024)
Objectives: Although some studies have evaluated the effectiveness of comprehensive genomic profiling (CGP) in solid tumors, the effectiveness of CGP in metastatic colorectal cancer (mCRC) has not been evaluated using detailed real-world long-outcome
Externí odkaz:
https://doaj.org/article/c07ff7079e574fd788b4a0358c9bde11
Autor:
Akinari Takao, Tatsuro Yamaguchi, Hidetaka Eguchi, Yasushi Okazaki, Hideki Ishikawa, Kiwamu Akagi, Hideyuki Ishida
Publikováno v:
Journal of the Anus, Rectum and Colon, Vol 8, Iss 4, Pp 348-355 (2024)
Objectives: Serrated polyposis syndrome (SPS) is a rare condition associated with an increased risk of colorectal cancer. However, the genetic basis of SPS in Japanese patients remains unclear. The present study therefore aimed to address this omissi
Externí odkaz:
https://doaj.org/article/9a45a94f576f47329ceb0a20ef4fe44f
Autor:
Hirotoshi Kobayashi, Kenjiro Kotake, Kotaro Maeda, Takeshi Suto, Masayasu Kawasaki, Hideki Ueno, Koji Komori, Heita Ozawa, Keiji Koda, Masayuki Ohue, Kimihiko Funahashi, Ichiro Takemasa, Hideyuki Ishida, Shinsuke Kazama, Yoshifumi Shimada, Hajime Morohashi, Yusuke Kinugasa, Yukihide Kanemitsu, Hiroki Ochiai, Soichiro Ishihara, Michio Itabashi, Kenichi Sugihara, Yoichi Ajioka
Publikováno v:
Annals of Gastroenterological Surgery, Vol 8, Iss 5, Pp 807-816 (2024)
Abstract Aim To clarify the usefulness of intraoperative lavage cytology in patients undergoing curative resection for pStage II‐III colorectal cancer in a prospective multicenter study. Methods Patients preoperatively diagnosed with stage II‐III
Externí odkaz:
https://doaj.org/article/55b693b722834f1a9578389232f52c7a
Autor:
Takatoshi Matsuyama, Hideyuki Ishida, Kazutaka Yamada, Kenichi Sugihara, Yoichi Ajioka, the Japanese Society for Cancer of the Colon and Rectum
Publikováno v:
Journal of the Anus, Rectum and Colon, Vol 8, Iss 3, Pp 163-170 (2024)
Objectives: Due to its rarity, there is insufficient evidence for managing ASCC patients with distant metastasis. Thus far, the therapeutic strategy for distant metastasis of ASCC is less standardized and requires a more individualized approach. Ther
Externí odkaz:
https://doaj.org/article/403bc1703df44d9e8bbe68a2b85fe1cf
Autor:
Tetsuji Takayama, Naoki Muguruma, Masahiro Igarashi, Shozo Ohsumi, Shiro Oka, Fumihiko Kakuta, Yoshiaki Kubo, Hideki Kumagai, Mika Sasaki, Tamotsu Sugai, Kokichi Sugano, Yuko Takeda, Hisashi Doyama, Kouji Banno, Suguru Fukahori, Yoichi Furukawa, Takahiro Horimatsu, Hideki Ishikawa, Takeo Iwama, Yasushi Okazaki, Yutaka Saito, Nariaki Matsuura, Michihiro Mutoh, Naohiro Tomita, Takashi Akiyama, Toshiki Yamamoto, Hideyuki Ishida, Yoshiko Nakayama
Publikováno v:
Journal of the Anus, Rectum and Colon, Vol 7, Iss 4, Pp 284-300 (2023)
Cowden syndrome (CS)/PTEN hamartoma tumor syndrome (PHTS) is a rare autosomal dominantly inherited condition caused by germline pathogenesis. It is associated with multiple hamartomatous lesions occurring in various organs and tissues, including the
Externí odkaz:
https://doaj.org/article/4255ab15b39b4693b801fad34a880813
Autor:
Akiko Miyazaki, Saori Itoi-Ochi, Mami Hayashi, Asako Ota, Kengo Nagai, Shinya Inoue, Naohiro Tomita, Hidetaka Eguchi, Yasushi Okazaki, Hideyuki Ishida, Takashi Hashimoto
Publikováno v:
Case Reports in Dermatology, Vol 15, Iss 1, Pp 126-132 (2023)
Linear IgA disease (LAD) is a rare autoimmune bullous disease characterized by IgA deposition in the basement membrane zone (BMZ). A 66-year-old male was treated for myelodysplastic syndrome at our hospital for 5 years, during which his condition rem
Externí odkaz:
https://doaj.org/article/07af11149fa34d82ba818474887b8941
Autor:
Hirotoshi Kobayashi, Kenjiro Kotake, Masayasu Kawasaki, Yukihide Kanemitsu, Yusuke Kinugasa, Hideki Ueno, Kotaro Maeda, Takeshi Suto, Michio Itabashi, Kimihiko Funahashi, Heita Ozawa, Fumikazu Koyama, Shingo Noura, Hideyuki Ishida, Masayuki Ohue, Tomomichi Kiyomatsu, Soichiro Ishihara, Keiji Koda, Hideo Baba, Kenji Kawada, Yojiro Hashiguchi, Takanori Goi, Yuji Toiyama, Naohiro Tomita, Eiji Sunami, Yoshito Akagi, Jun Watanabe, Kenichi Hakamada, Goro Nakayama, Kenichi Sugihara, Yoichi Ajioka
Publikováno v:
Annals of Gastroenterological Surgery, Vol 7, Iss 5, Pp 765-771 (2023)
Abstract Aim To establish a new Japanese classification of synchronous peritoneal metastases from colorectal cancer. Methods This multi‐institutional, prospective, observational study enrolled patients who underwent surgery for colorectal cancer wi
Externí odkaz:
https://doaj.org/article/74be57d7aca5465e89632fbb243dd8ab
Autor:
Takayuki Matsumoto, Junji Umeno, Keisuke Jimbo, Masami Arai, Itaru Iwama, Hiroshi Kashida, Takahiro Kudo, Koichi Koizumi, Yasushi Sato, Shigeki Sekine, Shinji Tanaka, Kohji Tanakaya, Kazuo Tamura, Keiji Hirata, Suguru Fukahori, Motohiro Esaki, Hideki Ishikawa, Takeo Iwama, Yasushi Okazaki, Yutaka Saito, Nariaki Matsuura, Michihiro Mutoh, Naohiro Tomita, Takashi Akiyama, Toshiki Yamamoto, Hideyuki Ishida, Yoshiko Nakayama
Publikováno v:
Journal of the Anus, Rectum and Colon, Vol 7, Iss 2, Pp 115-125 (2023)
Juvenile polyposis syndrome (JPS) is a rare disease characterized by multiple hamartomatous polyps within the gastrointestinal tract. SMAD4 or BMPR1A is known as a causative gene of JPS. Approximately 75% of newly diagnosed cases have an autosomal-do
Externí odkaz:
https://doaj.org/article/4303d107d2664da9b1128f48062decc5
Publikováno v:
Journal of the Anus, Rectum and Colon, Vol 7, Iss 2, Pp 38-51 (2023)
For nearly half a century, desmoid tumor (DT) has been considered a major complication that occurs in approximately 10%-25% of familial adenomatous polyposis (FAP) patients. It is also the leading cause of death in patients undergoing colectomy. We b
Externí odkaz:
https://doaj.org/article/48362048533341d586dc6f9b42be6d50