Zobrazeno 1 - 10
of 265
pro vyhledávání: '"Takashi Akiyama"'
Autor:
Kazuhiro Komi, MD, Minoru Fujita, MD, PhD, Noriaki Manabe, MD, PhD, Munenori Takaoka, MD, PhD, Katsuya Kato, MD, PhD, Hideyo Fujiwara, MD, PhD, Takako Konishi, MD, Emiko Bukeo, MD, Hiraku Misawa, MD, Jun Nakamura, MD, PhD, Maki Ayaki, MD, PhD, Takahisa Murao, MD, PhD, Mitsuhiko Suehiro, MD, PhD, Takashi Akiyama, MD, PhD, Hirofumi Kawamoto, MD, PhD, Tomoari Kamada, MD, PhD, Atsushi Urakami, MD, PhD, Yoshio Naomoto, MD, PhD, Tomoki Yamatsuji, MD, PhD, Takuya Moriya, MD, PhD, Ken Haruma, MD, PhD, Jiro Hata, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 9, Pp 3988-3993 (2024)
We herein report a case of sporadic intra-abdominal desmoid-type fibromatosis in which contrast-enhanced ultrasonography (US) combined with superb microvascular imaging (SMI) was useful for preoperative diagnosis. 18-Fluorodeoxyglucose positron emiss
Externí odkaz:
https://doaj.org/article/545a3d5f75354ad0aa5fe6bb173ee685
Autor:
Takako Konishi, Noriaki Manabe, Akihiro Shibuya, Emiko Bukeo, Jun Nakamura, Minoru Fujita, Hideyo Fujiwara, Yuko Fukuhara, Munenori Takaoka, Takashi Akiyama, Katsuya Kato, Jiro Hata, Ken Haruma, Tomoki Yamatsuji
Publikováno v:
Radiology Case Reports, Vol 19, Iss 4, Pp 1480-1483 (2024)
A 74-year-old man presented to the emergency department with the chief complaint of abdominal pain. A computed tomography scan showed paralytic ileus. An ileostomy tube was placed, but the symptoms of bowel obstruction did not improve. Two days after
Externí odkaz:
https://doaj.org/article/63041b35c2534f7eb7ffb79ee71e5838
Autor:
Seiya Hashimoto, Hirofumi Fukuda, Kohei Takeda, Keiichi Uchida, Fumiaki Sanuki, Takashi Akiyama, Eisei Kondo, Hideho Wada
Publikováno v:
Cancer Reports, Vol 7, Iss 2, Pp n/a-n/a (2024)
Abstract Background The main differences in cases of sudden elevation of hepatic enzyme levels during immunochemotherapy are the reactivation of the hepatitis B virus or drug‐induced liver injury. Here, we report a case of acute liver injury caused
Externí odkaz:
https://doaj.org/article/567cdf4be41e4e599912aa2739c341ae
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:
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
Autor:
Jun Nakamura, Noriaki Manabe, Tomoki Yamatsuji, Yoshinori Fujiwara, Takahisa Murao, Maki Ayaki, Minoru Fujita, Akiko Shiotani, Tomio Ueno, Yasumasa Monobe, Takashi Akiyama, Ken Haruma, Yoshio Naomoto, Jiro Hata
Publikováno v:
BMC Gastroenterology, Vol 22, Iss 1, Pp 1-9 (2022)
Abstract Background To date, no in-depth studies have focused on the impact of various clinical characteristics of esophageal squamous cell carcinoma (ESCC), including its association with subjective symptoms, on patient prognosis. We aimed to invest
Externí odkaz:
https://doaj.org/article/723b763a2d1c4a60aed045510cca475f
Autor:
Shunji Endo, Yoshinori Fujiwara, Koji Kurose, Masaharu Higashida, Hisako Kubota, Yuko Okamoto, Shumei Mineta, Hironori Tanaka, Toshimasa Okada, Atsushi Tsuruta, Takashi Akiyama, Toru Oga, Tomio Ueno
Publikováno v:
Surgical Case Reports, Vol 6, Iss 1, Pp 1-6 (2020)
Abstract Background Nivolumab is effective for gastric cancer and lung cancer, but complete response is rare. We experienced a case of synchronous gastric cancer and lung cancer who was treated by nivolumab and laparoscopic gastrectomy. Case presenta
Externí odkaz:
https://doaj.org/article/d4ff439622d44f05b66d62a84cc3550f
Publikováno v:
Case Reports in Pediatrics, Vol 2017 (2017)
Background. Situs inversus is a rare congenital anomaly with a reported incidence of only 1 in 5,000 to 10,000 live births. Congenital duodenal stenosis complicated with situs inversus is an even rarer entity. Case Presentation. A 1-year-old girl wit
Externí odkaz:
https://doaj.org/article/dc401d0ac40c44fbaa0c113fcb5cde4a
Autor:
Hiroshi Matsumoto, Yoshiki Kimura, Takahisa Murao, Motoyasu Osawa, Takashi Akiyama, Kiyohito Mannoji, Risa Koresawa, Hirotoshi Tokunaga, Hideho Wada, Takashi Sugihara, Ken Haruma
Publikováno v:
Case Reports in Gastroenterology, Vol 8, Iss 2, Pp 240-244 (2014)
Epstein-Barr virus (EBV) and cytomegalovirus (CMV) are members of the herpesvirus family and common causes of viral infection in humans. CMV infection of the gastrointestinal tract occurs mainly in immunocompromised individuals, on the other hand EBV
Externí odkaz:
https://doaj.org/article/fab7915ce1544a87ab41ecd0410149d2
Autor:
Hironori Yamamoto, Hirotsugu Sakamoto, Hideki Kumagai, Takashi Abe, Shingo Ishiguro, Keiichi Uchida, Yuko Kawasaki, Yoshihisa Saida, Yasushi Sano, Yoji Takeuchi, Masahiro Tajika, Takeshi Nakajima, Kouji Banno, Yoko Funasaka, Shinichiro Hori, Tatsuro Yamaguchi, Teruhiko Yoshida, Hideki Ishikawa, Takeo Iwama, Yasushi Okazaki, Yutaka Saito, Nariaki Matsuura, Michihiro Mutoh, Naohiro Tomita, Takashi Akiyama, Toshiki Yamamoto, Hideyuki Ishida, Yoshiko Nakayama
Publikováno v:
Digestion. :1-13
Background: Peutz-Jeghers syndrome (PJS) is a rare disease characterized by the presence of hamartomatous polyposis throughout the gastrointestinal tract, except for the esophagus, along with characteristic mucocutaneous pigmentation. It is caused by