Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Ryuta Saka"'
Autor:
Koichi Deguchi, Ryuta Saka, Miho Watanabe, Kazunori Masahata, Motonari Nomura, Masafumi Kamiyama, Takehisa Ueno, Yuko Tazuke, Hiroomi Okuyama
Publikováno v:
Surgical Case Reports, Vol 8, Iss 1, Pp 1-6 (2022)
Abstract Background Duplication cysts close to the ileocecal valve are usually treated with ileocecal resection. However, loss of the ileocecal valve will lead to problems, especially in infants. Mucosectomy of the cyst would be a better alternative
Externí odkaz:
https://doaj.org/article/87080d58025241d09e76aea06d057889
Publikováno v:
Surgical Case Reports, Vol 8, Iss 1, Pp 1-6 (2022)
Abstract Background Congenital tracheal stenosis (CTS) is a rare and life-threatening airway disorder, which is often associated with cardiac malformations. Among them, neonatal symptomatic CTS with cardiac malformations has an extremely poor prognos
Externí odkaz:
https://doaj.org/article/6d8a868665c94230b8e7b0634698141f
Autor:
Koichi Deguchi, MD, Yuko Tazuke, MD, PhD, Miho Watanabe, MD, PhD, Chiyoshi Toyama, MD, Motonari Nomura, MD, PhD, Ryuta Saka, MD, PhD, Hiromi Harada, Yukie Nagamine, Masayuki Endo, MD, PhD, Ritsuko Puh, MD, PhD, LLB, MSc, Hiroomi Okuyama, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 3, Pp 881-885 (2022)
Accessory scrotum (AS) is rarely diagnosed antenatally, and its prenatal features remain unknown. Here, we report a case of a prenatally diagnosed accessory scrotum with perineal lipoma. A 33-year-old woman was referred to our hospital at 35 weeks of
Externí odkaz:
https://doaj.org/article/8bdd3b99b7de4910b124c8874867e970
Autor:
Kazunori Masahata, Takehisa Ueno, Kazuhiko Bessho, Tasuku Kodama, Ryo Tsukada, Ryuta Saka, Yuko Tazuke, Shuji Miyagawa, Hiroomi Okuyama
Publikováno v:
Surgical Case Reports, Vol 8, Iss 1, Pp 1-6 (2022)
Abstract Background Progressive familial intrahepatic cholestasis (PFIC) is a heterogeneous group of genetic autosomal recessive diseases that cause severe cholestasis, which progresses to cirrhosis and liver failure, in infancy or early childhood. W
Externí odkaz:
https://doaj.org/article/59f124e00961488a9e6370bc4a229634
Publikováno v:
Surgical Case Reports, Vol 7, Iss 1, Pp 1-5 (2021)
Abstract Background Congenital pyloric atresia (CPA) is a rare gastrointestinal anomaly frequently associated with epidermolysis bullosa (EB). Although the complications of familial isolated CPA are minor, delays in diagnosis can increase the chances
Externí odkaz:
https://doaj.org/article/2d592b19af9c4642b9b1ace429dce3fb
Autor:
Ryuta Saka, Takaaki Sakai, Tomomitsu Kanaya, Yuko Tazuke, Yosuke Kugo, Masaki Taira, Takayoshi Ueno, Hiroomi Okuyama
Publikováno v:
Surgical Case Reports, Vol 6, Iss 1, Pp 1-5 (2020)
Abstract Background Diaphragmatic hernia is a rare complication of ventricular assist device (VAD), mainly developing after explantation of the device. We herein report a case of diaphragmatic hernia that developed following the implantation of VAD.
Externí odkaz:
https://doaj.org/article/521ed21a1f7f4621bee6d16da3b10a0e
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 17, Iss C, Pp 37-41 (2017)
A mature teratoma of the pancreas has rarely been reported, and postoperative superior mesenteric artery syndrome (SMAS) is extremely rare in pediatric pancreatic surgery. A 12-year-old girl underwent an enucleation of the large mature teratoma locat
Externí odkaz:
https://doaj.org/article/db11fff728eb4cafaa96f711297be689
Autor:
Ryuta Saka, Takashi Sasaki, Keigo Nara, Toshimichi Hasegawa, Satoko Nose, Hiroomi Okuyama, Takaharu Oue
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 3, Iss 8, Pp 351-355 (2015)
Transmesenteric hernia is abdominal visceral herniation through a congenital or acquired mesenteric defect. Treves' field is the area of terminal ileal mesentery circumscribed by the ileocolic artery and its last ileal branch. It is very susceptible
Externí odkaz:
https://doaj.org/article/09af030e80de4814addd287b41b0936b
Autor:
Shun Iwasaki, Takehisa Ueno, Chiyoshi Toyama, Koichi Deguchi, Motonari Nomura, Ryuta Saka, Miho Watanabe, Yuko Tazuke, Kazuhiko Bessho, Hiroomi Okuyama
Publikováno v:
Transplantation Proceedings. 54:552-555
Hepatopulmonary syndrome (HPS) is a disease of gas exchange caused by intrapulmonary shunting secondary to liver disease-associated intrapulmonary vascular dilation. HPS is characterized by the triad of cirrhosis, chronic liver disease, or portosyste
Autor:
Yuko Tazuke, Motonari Nomura, Yuki Noguchi, Tasuku Kodama, Yuichi Takama, Ryuta Saka, Takehisa Ueno, Hiroomi Okuyama, Kazuhiko Bessho
Publikováno v:
Pediatric Surgery International. 37:223-228
Portoenterostomy (PE) is the standard treatment for biliary atresia (BA). However, micro-bile ducts are difficult to identify with surgical loupes and dissect systematically. We report the effects of our attempts to dissect hilar tissue using a surgi