Zobrazeno 1 - 10
of 45
pro vyhledávání: ''
Publikováno v:
Journal of Pediatric Surgery. 51:2058-2062
Background Sarcoma accounts for 20% of solid tumors in children. Surgery has significant morbidity. We hypothesized that delivering chemotherapy directly into tumors through sustained release silk systems could slow tumor growth. Methods Human Ewing
Autor:
Min He, Jinhu Wang, Shan Xu, Jun-Qing Mao, Can Lai, Jiabin Cai, Qiang Shu, Min-Ju Li, Daxing Tang
Publikováno v:
Journal of pediatric surgery. 54(3)
Background Clear cell sarcoma of the kidney (CCSK) is a rare and aggressive malignant renal tumor. We describe our experience with neoadjuvant transcatheter arterial chemoembolization (TACE) and systematic chemotherapy for the treatment of advanced C
Autor:
Matthew J. Krasin, Mark A. Williams, Jeffrey S. Dome, Lisa M. McGregor, Kathleen Kieran, Andrew M. Davidoff
Publikováno v:
Journal of Pediatric Surgery. 49:149-153
Background Renal insufficiency is a significant complication of Wilms tumor treatment in the 5% with bilateral disease. Nephron-sparing surgery (NSS) is recommended after neoadjuvant chemotherapy initially. However, the role of NSS in recurrent disea
Autor:
Shambhunath Das, Arun Gupta, Gayatri S. Munghate, Dhananjay Malankar, Nidhi Sugandhi, Sandeep Agarwala, A. K. Bisoi
Publikováno v:
Journal of Pediatric Surgery. 46:2387-2390
Clear cell sarcoma of the kidney (CCSK) is a rare renal tumor. Only 4 cases of CCSK with vascular thrombus have been reported, and 2 of these were pediatric cases. One of the children had an intraatrial thrombus as well. We describe a 3-year-old boy
Publikováno v:
Journal of Pediatric Surgery. 46:978-982
Wilms' tumor is the most common malignant renal tumor of childhood. Surgical resection is an important aspect of therapy and is traditionally performed through an open transabdominal approach. The advent of advanced laparoscopic techniques for benign
Autor:
Mitsuru Muto, Toshiro Honna, Tatso Kuroda, Akihiro Fujino, Yoshihiro Kitano, Mureo Kasahara, Hideaki Tanaka
Publikováno v:
Journal of Pediatric Surgery. 46:973-977
Hepatocellular carcinoma (HCC) in children is rare, and the prognosis has been poor because of its advanced stage at diagnosis and unresponsiveness to chemotherapy. We report a 13-year-old boy with ruptured HCC in the left trisegment. When hemostasis
Autor:
Minoru Yagi, Atsushi Ogawa, Naoki Okuyama, Satoshi Kanada, Satoru Yamazaki, Teruhiro Watanabe, Masayuki Kubota, Yoshiaki Kinoshita, Keiko Asami
Publikováno v:
Journal of Pediatric Surgery. 39:1328-1332
Background/Purpose Before adopting a national protocol of aggressive chemotherapy for patients with advanced neuroblastoma in 1985, the treatment strategies in use varied considerably among the institutions in Japan. An aggressive surgical resection
Publikováno v:
Journal of Pediatric Surgery. 36:755-759
Background: The authors reviewed retrospectively their experience in 30 children with hepatoblastoma (HB). Despite an increased trend in the incidence of HB during the last 2 decades, an encouraging cure rate has been achieved with complete resection
Autor:
Pedram Argani, Elizabeth J. Perlman, J. Bruce Beckwith, Thomas E. Hamilton, Michael L. Ritchey, Cecilia A. Cotton, Robert C. Shamberger
Publikováno v:
Journal of Pediatric Surgery. 43:1982-1984
Purpose We reviewed the long-term local tumor control in patients with bilateral Wilm's tumor (BWT) who received no definitive surgical therapy to one kidney after complete radiographic resolution after initial chemotherapy. Methods National Wilm's T
Publikováno v:
Journal of Pediatric Surgery. 33:1771-1775
Background: The prognosis of hepatoblastoma is poor unless the tumor is completely resected. Various types of chemotherapy have been developed to increase its resectability. Recently, transcatheter arterial chemoembolization (TACE) has been developed