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Gastrointestinal stromal tumor presenting with prominent calcification 被引量:2
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作者 Naoki Izawa Takeshi Sawada +16 位作者 Ryuichi Abiko Daisuke Kumon Mami Hirakawa Mika Kobayashi Nobuyuki Obinata Masahito Nomoto Tadateru Maehata Shun-ichi Yamauchi Takefumi Kouro Takashi Tsuda Satoshi Kitajima Hiroshi Yasuda keiichi tanaka Ichiro tanaka Masahiro Hoshikawa Masayuki Takagi Fumio Itoh 《World Journal of Gastroenterology》 SCIE CAS CSCD 2012年第39期5645-5648,共4页
We present a rare case of a gastrointestinal stromal tumor (GIST) in the stomach with prominent calcifica-tion at presentation. A 61-year-old woman visited our hospital because of epigastric discomfort. A spherical ca... We present a rare case of a gastrointestinal stromal tumor (GIST) in the stomach with prominent calcifica-tion at presentation. A 61-year-old woman visited our hospital because of epigastric discomfort. A spherical calcified lesion with a diameter of about 30 mm was incidentally shown in the left upper quadrant on an abdominal X-ray. Computed tomography demonstrated that the tumor was growing from the upper gastric body, with calcification in the peripheral ring area. A laparoscopic partial gastrectomy was performed, and the resected specimen revealed a well-circumscribed tumor with exophytic growth from the gastric muscularis propria. Microscopic examination revealed spindle- shaped tumor cells with calcification and hemorrhage. Additionally, positive immunoreactivity of the tumor to KIT and CD34 and a low mitotic index resulted in the diagnosis of very low risk GIST. There are a few case reports of heavily calcified GIST, although solitary or punctate calcification of primary GIST has been reported in several case series. Dystrophic calcification of necrotic or degenerative tissue is the supposed cause of primary calcified GISTs. In contrast, appearance of calcification after administration of imatinib mesylate, which may be one indicator of disease response, is possibly caused by a different mechanism. 展开更多
关键词 胃肠道 钙化 间质 肿瘤生长 突出 有丝分裂指数 肿瘤细胞 CD34
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Preliminary Result of Hyperfractionated High-Dose Proton Beam Radiotherapy for Pediatric Skull Base Chordomas
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作者 Masashi Mizumoto Hiroyoshi Akutsu +9 位作者 Tetsuya Yamamoto Takashi Fukushima Yoshiko Oshiro Daichi Takizawa keiichi tanaka Masaaki Goto Toshiyuki Okumura Akira Matsumura Koji Tsuboi Hideyuki Sakurai 《Journal of Cancer Therapy》 2017年第4期327-332,共6页
Objective: Proton beam therapy (PBT) may provide good local control for skull base chordoma and reduced toxicities, especially for pediatric patients. Methods: We evaluated the efficacy and safety of hyperfractionated... Objective: Proton beam therapy (PBT) may provide good local control for skull base chordoma and reduced toxicities, especially for pediatric patients. Methods: We evaluated the efficacy and safety of hyperfractionated high-dose PBT in6 pediatric patients with newly-diagnosed skull basechordoma who were treated with PBT at our institute from 2011 to 2015. The patients were 5 males and one female, and the median age was 9 years old (range: 5 - 13). All patients received surgery before PBT. The median period between surgery and PBT was 57 days (range: 34 - 129 days). The treatment dose was 78.4 GyE in 56 fractions (twice per day). Results: All patients received PBT without severe acute toxicity. The median follow-up period was 27 months (range: 21 - 71 months). At the last follow-up, all patients were alive and all tumors were well controlled. Acute and late toxicities were generally acceptable, with only grade 1 and 2 events. Late toxicities included growth hormone abnormality and cortical hormone abnormality. One patient needed growth hormone and cortical hormone replacement therapy. Conclusion: Although the number of pediatric patients was small, our overall findings in the 6 cases indicate that hyperfractionated high-dose PBT is safe and effective for pediatric patients with skull base chordoma. 展开更多
关键词 CHORDOMA RADIOTHERAPY PROTON Beam Therapy PROTON RADIOTHERAPY PEDIATRICS
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Iguratimod, a Disease-Modifying Anti-Rheumatic Drug, Inhibits Osteoclastogenesis and Bone Resorption through Suppression of the Nuclear Factor of Activated T Cells Signaling Pathway
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作者 Jun Shiota Hidetoshi Murao +2 位作者 Akihiko Miura Masaaki Mikami keiichi tanaka 《Open Journal of Rheumatology and Autoimmune Diseases》 2016年第4期106-119,共14页
Introduction: The aim of this study was to observe an inhibition of bone resorption and osteoclastogenesis by iguratimod (IGU, T-614), a disease-modifying anti-rheumatic drug, using adjuvant-induced arthritis (AIA) ra... Introduction: The aim of this study was to observe an inhibition of bone resorption and osteoclastogenesis by iguratimod (IGU, T-614), a disease-modifying anti-rheumatic drug, using adjuvant-induced arthritis (AIA) rats and receptor activator of nuclear factor kappa-B ligand (RANKL)-stimulated RAW264.7 cells. Methods: The bone mineral density and 3D morphometric parameters of hind paws in AIA rats were measured using micro computed tomography (μCT) imaging. The activity of osteoclast cells was estimated based on tartrate-resistant acid phosphatase (TRAP) staining in specimens from the rats. In vitro TRAP activity was investigated using RANKL-stimulated RAW264.7 cells. The amount of nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 1 (NFATc1) protein was measured by western blot analysis. The expression of Nfatc1, its regulator genes, its upstream factors, and osteoclast-functional genes were investigated. Results: In addition to the suppression of bone resorption and lesions of bone trabeculae of AIA rats, IGU significantly decreased the number of TRAP-positive cells in the calcaneal bones. Moreover, this drug inhibited the differentiation of RANKL-stimulated RAW264.7 cells into osteoclasts, which were identified morphologically and functionally. IGU decreased the amount of NFATc1 protein and improved the altered expression of NFATc1-associated genes and osteoclast-functional genes. Conclusions: IGU suppressed osteoclastogenesis and bone resorption via the RANKL-NFATc1 pathway, suggesting such effect would be expected in clinical use. 展开更多
关键词 Bone Resorption IGURATIMOD NFATc1 OSTEOCLAST Rheumatoid Arthritis
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乐陶
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作者 keiichi tanaka 伏平 《现代装饰(家居)》 2013年第11期52-55,共4页
一件完美的陶瓷工艺品的制作加工过程严密而细致。首先是将瓷土淘成可用的瓷泥,并将其分割开来摞成柱状。然后,将摞好的瓷泥放入旋转转盘,用手和拉坯工具将瓷泥拉成瓷坯。拉好的瓷坯只是一个雏形,还需要根据所做的形状选取不同的印模,... 一件完美的陶瓷工艺品的制作加工过程严密而细致。首先是将瓷土淘成可用的瓷泥,并将其分割开来摞成柱状。然后,将摞好的瓷泥放入旋转转盘,用手和拉坯工具将瓷泥拉成瓷坯。拉好的瓷坯只是一个雏形,还需要根据所做的形状选取不同的印模,将瓷坯印成各种不同的形状,再将印好的瓷坯修刮整齐与匀称,用清水洗去尘土。然后,画坯、上釉与烧窑。瓷坯在窑内经受千度高温的烧炼后,最终成为精美的瓷器。来自日本的陶瓷艺术家Keiichi Tanaka,1979年出生于日本千叶,1999年就读于日本武藏野美术大学工业系室内与工艺美术设计专业,2003年毕业后留校,担任助教、助理研究员。 展开更多
关键词 陶瓷艺术家 画坯 烧窑 武藏野 拉坯 上釉 制作加工 工艺美术设计 日本千叶 Tanaka
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