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上皮瘤

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Results Among 85 cases, 46 cases were lipomas, Twenty-seven cases were sebaceous cysts, 19 cases were angeiomas, 8 cases were fibroids, 5 cases were ganglionic cysts, 3 cases were neurilemmomas,1 case was dermal nevus, 1 cases was fattey necrosis, 1 case was adipositis, 1 case was foreign-body granuloma,1 case was calcified epithelioma.

结果 85例中脂肪瘤46例,皮脂腺囊肿27例,血管瘤19例,纤维瘤8例,腱鞘滑液囊肿5例,神经鞘膜瘤3例,皮肤痣、脂肪坏死、脂膜炎、异物肉芽肿、钙化上皮瘤各1例。

Results 86 cases were of pilomatrixoma (71.1%),11 cases of trichoepithelioma (9.1%),1 case was of desmoplastic trichoepithelioma,2 cases of trichoblastoma,5 cases of dilaled pore and pilar sheath acanthoma、1 case was of follicular toumor,3 cases of trichofolliculoma,3 cases of proliferating folliculas cyst and proliferating tricholemmoma,6 cases of tricholemmoma of pilar sheath adrentitial.

结果 毛母质瘤86例(71.1%)、毛发上皮瘤11例(9.1%)、促结缔组织增生性毛发上皮瘤1例、毛母细胞瘤2例、圆锥漏斗状棘皮瘤与毛鞘棘皮瘤5例、毛囊漏斗肿瘤1例、毛发滤泡瘤与毛发滤泡癌3例、增生性毛囊囊肿与增生性外毛根鞘瘤3例、毛鞘瘤与毛鞘癌6例。

Results Among 85 cases, 46 cases were lipomas, Twenty-seven cases were sebaceous cysts, 19 cases were angeiomas, 8 cases were fibroids, 5 cases were ganglionic cysts, 3 cases were neurilemmomas,1 case was dermal nevus, 1 cases was fattey necrosis, 1 case was adipositis, 1 case was foreign-body granuloma,1 case was calcified epithelioma.

回顾性分析85例体表良性肿块的超声表现,总结其声像图特征,所有病例均经手术病理证实。结果 85例中脂肪瘤46例,皮脂腺囊肿27例,血管瘤19例,纤维瘤8例,腱鞘滑液囊肿5例,神经鞘膜瘤3例,皮肤痣、脂肪坏死、脂膜炎、异物肉芽肿、钙化上皮瘤各1例。

The most common types are Meibomian gland adenoma, papilloma, melanoma (eyelid, conjunctiva, sclera, iris, ciliary body, choroid), squamous cell carcinoma, adenoma, adenocarcinoma, lymphoma, medulloepithelioma, ganglioglioma, osteosarcoma, mast cell tumor, and optic nerve sheath meningioma.

最常见的类型是睑板腺腺瘤,乳头状瘤,黑色素瘤(眼睑,结膜,虹膜,睫状体,脉络膜),鳞状细胞癌,腺瘤,腺癌,淋巴瘤(视网膜,脉络膜,睫状体),髓上皮瘤,神经节胶质瘤,骨肉瘤,肥大细胞瘤和视神经鞘脑膜瘤。

At histopathologic analysis, neuronal tumors are usually classified as pure neuronal cell tumors (gangliocytoma, Lhermitte-Duclos disease , central neurocytoma) and mixed neuronal-glial tumors (ganglioglioma, desmoplastic infantile ganglioglioma, dysembryoplastic neuroepithelial tumor, ganglioneuroma).

根据组织病理学的分析,神经元肿瘤通常被分为:单纯的神经元细胞肿瘤(神经节细胞瘤,Lhermitte-Duclos 病〔发育不良性小脑神经节细胞〕瘤),中枢神经细胞瘤)和混合性的神经元-胶质肿瘤(神经节神经胶质瘤,成结缔组织性婴儿节细胞胶质瘤,胚胎发育不良性神经上皮瘤,神经节瘤)。

Results: The findings on CT and MRI were as follows: 57 cases of Oligodendroglioma, 15 cases of Ganglioglioma , 5 cases of Dysembryoplastic neuroepithelial tumor , 3 cases of Pleomorphic xanthoastrocytoma .

结果:少枝胶质瘤47例,间变性少枝胶质瘤10例,节细胞胶质瘤15例,胚胎发育不良性神经上皮瘤5例,多形黄色细胞瘤3例。

Results: the findings on ct and mri were as follows: 57 cases of oligodendroglioma, 15 cases of ganglioglioma , 5 cases of dysembryoplastic neuroepithelial tumor , 3 cases of pleomorphic xanthoastrocytoma .conclusion:the images on ct and mri of cerebra peripheral tumor occur some characters , so ct and mri were certain worth on the diagnose and differentiate diagnose of cerebra peripheral tumor.

结果:少枝胶质瘤47例,间变性少枝胶质瘤10例,节细胞胶质瘤15例,胚胎发育不良性神经上皮瘤5例,多形黄色细胞瘤3例。结论:脑浅表肿瘤存在影像特征,ct及mri对其诊断有一定的价值。少枝胶质细胞瘤;节细胞肿瘤;胚胎发育不良性神经上皮瘤;多形性黄色星形细胞瘤;ct;mri

Results 531 cases postoperatively diagnosed as endometriotic cyst,254 cases teratoma,139 inflammatory masses,121 serous cystademona,67 cases mucinous cystadenoma,128 parovarian,140 simple ovarian cyst,3 cases brenner tumor,1 case borderline mucinous cystadenoma,1 case mucinous cystadenocarcinoma,1 case endometrioid carcinoma and 1 case malignant brenner tumor.

结果术后诊断卵巢内膜异位囊肿 5 3 1例、卵巢畸胎瘤 2 5 4例、炎性肿块 13 9例、卵巢浆液性囊腺瘤 12 1例、卵巢粘液性囊腺瘤 67例、输卵管系膜囊肿 12 8例、卵巢单纯性囊肿 14 0例、卵巢纤维上皮瘤 3例、粘液性交界性囊腺瘤 1例、粘液性囊腺癌 1例、卵巢子宫内膜样癌 1例、卵巢恶性纤维上皮瘤 1例。

Part I :Multiple familial trichoepithelioma: Analyses of Clinical and Genetic Features Objective To study the clinical and genetic features of multiple familial trichoepithelioma in Chinese.

第一部分:多发性家族性毛发上皮瘤的遗传特征分析目的了解中国人多发性家族性毛发上皮瘤的临床表现和遗传特点。

Multiple family trichoepithelioma is a genetically heterogeneous disorder.

未发现本家族性毛发上皮瘤家系CYLD1基因第16、18号外显子存在突变,提示家族性毛发上皮瘤具有遗传异质性。

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