Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Noboru Oyachi"'
Publikováno v:
Surgical Case Reports, Vol 9, Iss 1, Pp 1-5 (2023)
Abstract Background Perforation of the pyriform sinus, included in hypopharyngeal injury, is a rare condition typically caused by iatrogenic factors. We present a case of an infant who developed deep cervical and mediastinal abscesses due to a trauma
Externí odkaz:
https://doaj.org/article/d7de1248b4d24010858d3704e6535257
Publikováno v:
Surgical Case Reports, Vol 8, Iss 1, Pp 1-6 (2022)
Abstract Background Congenital diaphragmatic hernia (CDH) is sometimes associated with complications involving herniation of intrathoracic organs, which further increase mortality rate. We encountered a case of postoperative gastric and splenic volvu
Externí odkaz:
https://doaj.org/article/e5440f22a17046c5bc81e2e9d1dd85ba
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-6 (2022)
Abstract Background Psychological stress has been reported to cause hyperthermia. Persistent excessive hyperthermia can, in turn, cause hypercytokinemia and organ damage. We report a case of postoperative severe hyperthermia leading to a systemic inf
Externí odkaz:
https://doaj.org/article/8376eeadfecc4a9c9bc2becba8e5f55d
Publikováno v:
Surgical Case Reports, Vol 8, Iss 1, Pp 1-6 (2022)
Abstract Background A multiseptate gallbladder is a very rare congenital malformation in which the lumen is divided into variously sized multiseptal compartments. The pathogenesis and natural history of this disease remain uncertain. We herein descri
Externí odkaz:
https://doaj.org/article/3283fa597f9f451e971a45f769cf4835
Autor:
Tamao Shinohara, Yohei Hasebe, Daisuke Watanabe, Tomohide Sakurayama, Yuki Maebayashi, Fuminori Numano, Tomohiro Saito, Keiichi Koizumi, Atsushi Nemoto, Akitoshi Saito, Toshio Oyama, Noboru Oyachi, Minako Hoshiai, Atsushi Naitoh
Publikováno v:
Clinical Case Reports, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract Acquired cystic lung disease in premature infants is a serious respiratory complication, and pulmonary interstitial emphysema (PIE) has been widely reported. We report a rare case of giant pulmonary bulla in an infant treated with bullectomy
Externí odkaz:
https://doaj.org/article/b3f72ec5c7b145429cfdfdff405a0794
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 84, Iss , Pp 102387- (2022)
Congenital diaphragmatic hernia (CDH) is a common cause of neonatal mortality. If CDH is associated with non-immune fetal hydrops (FH), the mortality rate is even higher. However, the pathogenesis and management of FH associated with CDH are still un
Externí odkaz:
https://doaj.org/article/85f158cc3b524beea973c08c3f5adae1
Publikováno v:
Surgical Case Reports, Vol 7, Iss 1, Pp 1-5 (2021)
Abstract Background Several reports have documented that the pulmonary sequestration is in communication with the gastrointestinal tract and the concept of bronchopulmonary foregut malformation (BPFM) has become more widespread. However, there are fe
Externí odkaz:
https://doaj.org/article/debf157cc9ee40e9aa51e9c77a8780c1
Publikováno v:
Surgical Case Reports, Vol 5, Iss 1, Pp 1-5 (2019)
Abstract Background Non-occlusive mesenteric ischemia (NOMI) is a rare and severe pathological condition that can cause intestinal necrosis without mechanical obstruction of the mesenteric artery. NOMI often develops during the treatment of severe di
Externí odkaz:
https://doaj.org/article/3c3f1aec52b84683939f48e86fba07e1
Autor:
Noboru Oyachi, Takeyuki Suzuki, Takaki Emura, Kazuko Obana, Atsushi Nemoto, Atsushi Naito, Toshio Oyama
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 30, Iss C, Pp 1-3 (2018)
Segmental absence of intestinal musculature is a rare condition. A female patient was born at 39 weeks gestational age with birth weight of 2,900 g. The patient was prenatally diagnosed as having segmental bowel distension in the fetal stage. She man
Externí odkaz:
https://doaj.org/article/2b0446e591c840dd8785917f0b62dc53
Publikováno v:
CEN Case Rep
A caliceal diverticulum is a rare entity in children. Its etiology is closely associated with that of ureteropelvic junction malformations and renal dysplasia. We herein present a case of these complex disorders in an infant. A renal cyst and hydrone