Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Toshiji Nishi"'
Autor:
Yokatsu Ohama, Yasunori Toyoda, Keisuke Kato, Shigeharu Okuzumi, Yukichi Tanaka, Kenji Kurosawa, Noriko Aida, Toshiji Nishi, Noriyuki Nagahara, Hisato Kigasawa, Mio Tanaka
Publikováno v:
Pathology - Research and Practice. 209:309-313
Synovial sarcoma, which is difficult to diagnose precisely, is one of the most common childhood nonrhabdomyosarcoma soft-tissue sarcomas. The purpose of this study is to develop new molecular cytogenetic assay. We used two sets of two-color break-apa
Autor:
Yukichi Tanaka, Masato Shinkai, Hiroshi Take, Noriko Aida, Masataka Adachi, Shoji Takemiya, Hiroshi Yamamoto, Youkatsu Ohhama, Toshiji Nishi, Katsuhiko Tachibana, Shogo Fujita, Keisuke Kato
Publikováno v:
Journal of Pediatric Surgery. 36:1026-1031
Background/Purpose: Congenital absence of the portal vein (CAPV) is a subtype of congenital portosystemic shunt, which can cause a broad spectrum of clinical manifestations. The authors report on 4 patients with CAPV including a boy with CAPV-associa
Publikováno v:
Journal of Pediatric Surgery. 35:1031-1034
Background/Purpose: The aim of this study was to determine early prognostic indicators forthe prediction of long-term survival rate and timing of the liver transplantation after the Kasai operation. Methods: A retrospective chart study was performed
Autor:
Yasunori Toyoda, Toshiji Nishi, Hisato Kigasawa, Hirokazu Nishihira, Takashi Momoi, Yukichi Tanaka, Rieko Ijiri, Noriko Aida, Maho Takeuchi, Kazuaki Misugi, Keisuke Kato
Publikováno v:
The American Journal of Surgical Pathology. 24:807-815
Spontaneous regression and maturation of neuroblastoma (NB) are well documented and occur frequently in infants, including those detected by mass screening. To seek histologic clues for regression/maturation in mass-screened NB, clinicopathologic fea
Autor:
Toshiji Nishi, Masahiko Maie, Akira Hayashi, Morihiro Saeki, Masao Endo, Michiomi Ishihara, Akira Nagasaki
Publikováno v:
Journal of Pediatric Surgery. 34:435-441
Background/Purpose: This report describes the results of a group study of the Japanese Study Group of Anorectal Anomolies (JSGA) to determine the relative incidence of specific types of anorectal anomaly in Japan, and includes discussion of rectouret
Autor:
Masato Shinkai, Makoto Akaike, Yukio Sugimasa, Youkatsu Ohhama, Syogo Fujita, Hiroshi Yamamoto, Syoji Takemiya, Hiroyasu Tanabe, Akio Satoh, Toshiji Nishi, Katsuyuki Torigai
Publikováno v:
Surgery Today. 28:173-177
With the cooperation of surgeons in two separate institutes, living-related donor liver transplantation was safely performed at the Kanagawa Children's Medical Center. The donor operations were carried out at Kanagawa Cancer Center by surgeons of the
Autor:
Kiyoshi Imaizumi, Toshiji Nishi, Yohei Miyagi, Ichiro Aoki, Hirokazu Nishihira, Yoji Nagashima, Yoshiro Sasaki, Yukichi Tanaka, Kazuaki Misugi
Publikováno v:
Cancer. 77:799-804
BACKGROUND. A candidate tumor suppressor gene, WT-1, is believed to have an important role in the pathogenesis of Wilms' tumor, especially that occurring in patients with congenital aniridia. METHODS. To obtain a stable tumor line to work with, Wilms
Autor:
Yukichi Tanaka, Shosuke Imai, Yukio Hyodo, Hiroko Kurozumi, Toyoro Osato, Yukio Nakatani, Yoshiroh Sasaki, Toshiji Nishi
Publikováno v:
The American Journal of Surgical Pathology. 18:623-631
We report a pulmonary angiocentric immunoproliferative lesion (AIL) in an 11-year-old boy with chronic active Epstein-Barr virus (EBV) infection. The phenotypes of the proliferating lymphoid cells in the biopsied pulmonary lesion were CD2+, CD3+, CD4
Autor:
Yukichi Tanaka, Rieko Ijiri, Toshiji Nishi, Noriko Aida, Yasunori Toyoda, Kumiko Ishikawa, Keisuke Kato, Hisato Kigasawa, Junichi Hara, Takeshi Kusafuka
Publikováno v:
Journal of Pediatric Surgery. 36:953-955
The authors present unusual clinicopathologic findings of a patient with neuroblastoma stage 4S that recurred 11 years after induction of complete remission with chemotherapy. A 12-year-old girl presented with recurrent tumor in the liver. Urinary ca
Publikováno v:
Medical and Pediatric Oncology. 33:580-582