胆管瘤
胆管瘤的相关文献在1988年到2008年内共计90篇,主要集中在肿瘤学、外科学、预防医学、卫生学
等领域,其中期刊论文88篇、会议论文2篇、专利文献10542篇;相关期刊43种,包括中国超声医学杂志、临床肝胆病杂志、腹部外科等;
相关会议1种,包括全国肿瘤高发现场建设经验交流会等;胆管瘤的相关文献由146位作者贡献,包括蔡景修、黄志强、王敖川等。
胆管瘤—发文量
专利文献>
论文:10542篇
占比:99.15%
总计:10632篇
胆管瘤
-研究学者
- 蔡景修
- 黄志强
- 王敖川
- 黄洁夫
- 吴一武
- 周宁新
- 寿才灿
- 施维锦
- 曹绣虎
- 李升平
- 李维华
- 李荫山
- 王光升
- 钱光相
- 陈孝平
- 陈春蕾
- 顾红光
- André Roy
- Basilios Papaziogas
- Bich N Nguyen
- Fujito Kageyama
- George Basdanis
- George Paraskevas
- George Paroutoglou
- Giorgia Karagiannoulou
- Grigorios Chatzimavroudis
- Hirotoshi Nakamura
- Masataka Kikuyama
- Otmane Nafidi
- Panagiotis Katsinelos
- Shinichi Sumiyoshi
- Taxiarchis Katsinelos
- Yoshihiro Ide
- Yoshimasa Kobayashi
- Yuji Matsubayashi
- 丁显仲
- 丁重川
- 于皆平
- 付苓
- 何水兴
- 冯变喜
- 冯远德
- 刘向阳
- 刘振春
- 刘继炎
- 刘铁
- 初铭忠
- 吕保华
- 吴孟超
- 吴白云
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Otmane Nafidi;
Bich N Nguyen;
André Roy
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摘要:
Von Hippel-Lindau syndrome (VHL) is a rare autosomal-dominant, inherited familial cancer syndrome. Hemangioblastomas, pheochromocytomas and renal carcinoma are the frequent reported VHL tumors. Neuroendocrine tumors have also been described, mostly in the pancreas and rarely in the biliary trees. We report the second case of bile duct carcinoid in a 31-year-old VHL woman. She underwent right adrenalectomy for a pheochromocytoma in the past. She also had a positive family history of phenotypic expression of VHL syndrome. The patient presented with biliary colic. Endoscopic retrograde cholangio-pancreatography showed intra-luminal bile duct mass. Surgical exploration identified a beige nodular lesion that was a carcinoid tumor on histology. This new association should be clarified by further genetic investigations.
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Shinichi Sumiyoshi;
Masataka Kikuyama;
Yuji Matsubayashi;
Fujito Kageyama;
Yoshihiro Ide;
Yoshimasa Kobayashi;
Hirotoshi Nakamura
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摘要:
We report an extremely rare case where a mesenchymal differentiation, especially embryonal sarcoma, was demonstrated in cholangiocarcinoma. At autopsy, a yellowish-white tumor (15 cm x 12 cm) was found in the right hepatic lobe, and there were several daughter nodules in both hepatic lobes. Histologically, most of the main tumor and all of the daughter nodules examined showed sarcomatous changes (spindle cells, pleomorphic cells and hyalization). Histologic examination of a part of the main tumor disclosed a focus of adenocarcinoma within the tumor. The frequent transitions between the adenocarcinomatous areas and the sarcomatous areas suggested that sarcomatous transformation occurred in the cholangiocarcinoma and then spread rapidly. Immunohistochemically, the adenocarcinomatous elements were positive for cytokeratin, carcinoembryonic antigen (CEA) and epithelial membrane antigen, and negative in the sarcomatous cells. Vimentin was positive only in the sarcomatous elements. The findings of the present case support the view that carcinosarcomas represent carcinomas that develop sarcomatous elements via metaplasia of the epithelial element.
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管红梅;
杨亚芳;
承禾;
李海歌
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摘要:
@@ 肝门部胆管癌或称近端胆管癌,是肝门区引起恶性梗阻性黄疸常见肿瘤之一,约占肝外胆道肿瘤总数的62%.有关肝门部胆管癌螺旋CT三期(动脉期、门脉期、延迟期)增强的表现和诊断,国内外的文献报道很少.
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