Shun Iwasaki
Shun Iwasaki has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
Ryo Tsukada
Department of Pediatric Surgery, NHO Fukuyama Medical Center, 4-14-17 Okinogamicho, Fukuyama, Hiroshima 720-8520, Japan
2 shared publications- Ryuta Saka
Department of Pediatric Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan
2 shared publications - Taku Yamamichi
Department of Pediatric Surgery, Osaka Women’s and Children’s Hospital, Izumi, Japan
2 shared publications - Hiroomi Okuyama
Department of Pediatric Surgery, Osaka University Graduate School of Medicine, Osaka, Japan
1 shared publication - Koichi Deguchi
Department of Pediatric Surgery, Graduate School of Medicine, Osaka University, Osaka, Japan
1 shared publication Rika Omote
Department of Pathology, National Hospital Organization Fukuyama Medical Center, 14-17 Okinogamicho, Fukuyama, Hiroshima 720-0825, Japan
1 shared publication
Latest Publications
- Open Access
- 3 June 2026
- Published by Elsevier in Radiology Case Reports
- Vol. 21 (9) , 3597-3602
Sequential imaging approach with lymphoscintigraphy and intraoperative indocyanine green lymphography for refractory chylous ascites in an infant: A case report
- 3 June 2026
- Published by Elsevier in Radiology Case Reports
- Vol. 21 (9) , 3597-3602
Open AccessSequential imaging approach with lymphoscintigraphy and intraoperative indocyanine green lymphography for refractory chylous ascites in an infant: A case report
- Open Access
- 17 September 2025
- Published by Elsevier in Radiology Case Reports
- Vol. 20 (12) , 5989-5993
Multiseptate gallbladder with gallstones in a pediatric patient
- 17 September 2025
- Published by Elsevier in Radiology Case Reports
- Vol. 20 (12) , 5989-5993
Open AccessMultiseptate gallbladder with gallstones in a pediatric patient
- Open Access
- 29 February 2024
- Published by MDPI AG in Bioengineering
- Vol. 11 (3) , 243
Regeneration Process of an Autologous Tissue-Engineered Trachea (aTET) in a Rat Patch Tracheoplasty Model
The treatment of long-tracheal lesion is difficult because there are currently no viable grafts for tracheal replacement. To solve this problem, we have developed an autologous Tissue-Engineered Trachea (aTET), which is made up of collagenous tissues and cartilage-like structures derived from rat chondrocytes. This graft induced successful long-term survival in a small-animal experiment in our previous study. In this study, we investigated the regeneration process of an aTET to attain reproducible success. We prepared an aTET by using a specially designed mold and performed patch tracheoplasty with an aTET. We assigned twenty-seven rats to three groups according to the three types of patch grafts used: aTET patches (the aTET group), fresh tracheal autograft patches (the Ag group), or polylactic acid and polycaprolactone copolymer sheets (the PPc group). In each group, gross and histological evaluations were performed at 1 month (n = 3), 3 months (n = 3), and 6 months (n = 3) after implantation. We obtained high survival rates in all groups, but only the PPc group attained thick tracheal walls with granular tissues and no tracheal regeneration. On the other hand, the aTET and Ag groups reproducibly achieved complete tracheal regeneration in 6 months. So, an aTET could be a promising candidate for tracheal regeneration grafts.
- 29 February 2024
- Published by MDPI AG in Bioengineering
- Vol. 11 (3) , 243
Open AccessRegeneration Process of an Autologous Tissue-Engineered Trachea (aTET) in a Rat Patch Tracheoplasty Model
The treatment of long-tracheal lesion is difficult because there are currently no viable grafts for tracheal replacement. To solve this problem, we have developed an autologous Tissue-Engineered Trachea (aTET), which is made up of collagenous tissues and cartilage-like structures derived from rat chondrocytes. This graft induced successful long-term survival in a small-animal experiment in our previous study. In this study, we investigated the regeneration process of an aTET to attain reproducible success. We prepared an aTET by using a specially designed mold and performed patch tracheoplasty with an aTET. We assigned twenty-seven rats to three groups according to the three types of patch grafts used: aTET patches (the aTET group), fresh tracheal autograft patches (the Ag group), or polylactic acid and polycaprolactone copolymer sheets (the PPc group). In each group, gross and histological evaluations were performed at 1 month (n = 3), 3 months (n = 3), and 6 months (n = 3) after implantation. We obtained high survival rates in all groups, but only the PPc group attained thick tracheal walls with granular tissues and no tracheal regeneration. On the other hand, the aTET and Ag groups reproducibly achieved complete tracheal regeneration in 6 months. So, an aTET could be a promising candidate for tracheal regeneration grafts.