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1)  Trans-orbitozygomatic approach
颅底贯通性肿瘤
2)  communicated skull base tumor
颅底沟通性肿瘤
1.
A case report of communicated skull base tumor with initial manifestation as otitis media with effusion;
首发表现为渗出性中耳炎的颅底沟通性肿瘤
3)  Transcranial base tumors
颅底内外沟通性肿瘤
4)  skull base neoplasm
颅底肿瘤
1.
Study on the application of neuronavigation fusion in management of skull base neoplasm;
神经导航融合技术在颅底肿瘤中的应用
5)  Skull base tumor
颅底肿瘤
1.
Selection of operative approaches and reconstruction of the anterior skull base tumor;
前颅底肿瘤的术式选择及颅底重建
2.
Microsurgery resection of the skull base tumor under assisted neuronavigation;
神经导航辅助颅底肿瘤显微外科切除
3.
Changes of endothelin-1 and calcitonin gene-related peptide in plasma of cerebral vasospasm after resection of skull base tumors and the relation between the two factors and cerebral vasospasm;
颅底肿瘤术后血浆内皮素-1、降钙素基因相关肽的动态变化及其与脑血管痉挛的相关性
6)  skull base neoplasms
颅底肿瘤
1.
Clinical application of spiral CT angiography in the skull base neoplasms;
螺旋CT血管造影在颅底肿瘤中的应用价值
补充资料:卵巢混合性生殖细胞-性索间质性肿瘤


卵巢混合性生殖细胞-性索间质性肿瘤


  本瘤1921年首次由Masson描述,直到1972年由Telerman首次命名为本瘤,并沿用至今,本瘤病因尚不明了。发生年龄自新生儿到67岁妇女均可发生,少数为男性。临床表现:患者为正常女性及男性外表,女性病人可有下腹包块,发生蒂扭转时有下腹痛,并有急腹症症状,可有内分泌紊乱,性早熟表现,男性有睾丸增大。染色体核型分析均正常。内分泌检查与临床表现符合,肿瘤为单侧,圆形或卵圆形。表面光滑,直径2.5~30cm,实性肿瘤内有囊性区。切面灰白、灰红或淡黄至淡褐色。镜下有梭形细胞及生殖细胞。治疗:视情况采取单纯手术,或手术加放疗及化疗。需长期随访。预后:单纯本病者良好。
  
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