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primary vitreous
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  初发玻璃体
     Forty-five out of 45 retinoblastoma patients studied with high resolution computed tomography at the Hospital For Sick Children, Toronto, Canada, showed evidence of intraocular calcification. Simulating lesions such as Coat's disease, persistent hyperplastic primary vitreous (PHPV), toxocara, dominant exudative vitreal retinopathy (DEVR) and choroidal juvenile xanthogranuloma failed to demonstrate any calcifications. Thus in young patients in whom retinoblastoma is suspected, the presence of calcification on CT scan is diagnostic of retinoblastoma;
     在加拿大多伦多儿童病院,用高分辨力CT研究了45例视网膜母细胞瘤病人,均显示有眼内钙化的表现,而其他相类似的病变,如Coats病,永存性初发玻璃体增生症(PHPV),弓蛔虫病,显性渗出性玻璃体视网膜病变(DEVR)以及青少年性脉络膜黄色肉芽肿等,没有看到任何钙化的征象,故此,年幼病人疑为视网膜母细胞瘤时,CT检查如能显示钙化,则可作出诊断,否则,可能是其他相类似的病变。
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  “primary vitreous”译为未确定词的双语例句
     persistance of primary vitreous body 5 cases;
     原始玻璃体存留5例;
短句来源
     CT Diagnosis of Persistent Hyperplastic Primary Vitreous
     永存原始玻璃体增生症的CT诊断
短句来源
     The imaging features were analysed. Results Totally there were 5 cases of persistent hyperplastic primary vitreous,9 cases of premature with retinopathy,34 cases of retinoblastoma,3 cases of Coat’s disease,23 cases of nanophthalmus,16 cases of vitreous bleeding and 5 cases of endophalmitis.
     结果95例包括永存原始玻璃体增生症5例,早产儿视网膜病变9例,视网膜母细胞瘤34例,Coat’s病3例,小眼球23例(其中玻璃体密度正常13例,密度增高10例),玻璃体出血16例以及眼内炎5例。
短句来源
     Imaging of Persistent Hyperplastic Primary Vitreous(PHPV)
     原始永存玻璃体增生症(PHPV)的影像学
短句来源
     Color Doppler Imaging of Persistent Heperplastic Primary Vitreous
     永存性原始玻璃体增殖症的彩色多普勒成像特征
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  相似匹配句对
     Imaging of Persistent Hyperplastic Primary Vitreous(PHPV)
     原始永存玻璃体增生症(PHPV)的影像学
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     persistance of primary vitreous body 5 cases;
     原始玻璃体存留5例;
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     primary prevention.
     初级预防。
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     Will is primary.
     意志是第一性的,理性则是由意志派生出来的,理性命定为意志服务。
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  primary vitreous
Anomalous vitreous adhesion over the posterior retina could be related to the malformative genesis of the syndrome, and the anomalous persistence of the Cloquet's canal or primary vitreous could be responsible for the traction.
      
At birth the patient presented with right microphthalmia, right microcornea, and persistent hyperplastic primary vitreous of the right eye.
      
She had marked mental and physical retardation, generalized hypertonia, microphthalmia with persistent hypoplastic primary vitreous, blepharochalasia, high nasal bridge, micrognathia, malformed ears with preauricular pits, and overlying fingers.
      
There was corneal opacity with anterior segment dygenesis in the left eye, and persistent pupillary membrane, cataract and persistent hyperplastic primary vitreous in the right eye.
      
This study provides scanning electron microscopic observations on the early morphogenesis of persistent hyperplastic tunica vasculosa lentis and primary vitreous (PHTVL/PHPV) in canine fetuses at days 28 35 postcoitum (D28 and D35).
      
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Computerized tomography (CT)is important in the detection and clinical differentiation of retinoblastoma from other simulating lesions which present as leukocoria. Forty-five out of 45 retinoblastoma patients studied with high resolution computed tomography at the Hospital For Sick Children, Toronto, Canada, showed evidence of intraocular calcification. Simulating lesions such as Coat's disease, persistent hyperplastic primary vitreous (PHPV), toxocara, dominant exudative vitreal retinopathy (DEVR) and...

Computerized tomography (CT)is important in the detection and clinical differentiation of retinoblastoma from other simulating lesions which present as leukocoria. Forty-five out of 45 retinoblastoma patients studied with high resolution computed tomography at the Hospital For Sick Children, Toronto, Canada, showed evidence of intraocular calcification. Simulating lesions such as Coat's disease, persistent hyperplastic primary vitreous (PHPV), toxocara, dominant exudative vitreal retinopathy (DEVR) and choroidal juvenile xanthogranuloma failed to demonstrate any calcifications. Thus in young patients in whom retinoblastoma is suspected, the presence of calcification on CT scan is diagnostic of retinoblastoma; patients without calcification on CT probably have a simulating lesion.

CT在视网膜母细胞瘤与其他出现白瞳症的相象的病变的检查和鉴别诊断方面具有重要意义。在加拿大多伦多儿童病院,用高分辨力CT研究了45例视网膜母细胞瘤病人,均显示有眼内钙化的表现,而其他相类似的病变,如Coats病,永存性初发玻璃体增生症(PHPV),弓蛔虫病,显性渗出性玻璃体视网膜病变(DEVR)以及青少年性脉络膜黄色肉芽肿等,没有看到任何钙化的征象,故此,年幼病人疑为视网膜母细胞瘤时,CT检查如能显示钙化,则可作出诊断,否则,可能是其他相类似的病变。

The ultrasonic diagnosis of 1227 eye patients(1395 eyes)were reported.Among them,intraocular foreign bodies 20.29%,vitreous hemorrhage and opacity 15.56%,retinal detachment 12.76%,proliferative retinopathy 10. 25%,aphakia 8.24%,retinoblastoma 3.15%, ocular atrophy 2.80%.Rare disease of the eye included:scleral staphyloma,retrolental fibroplasia, dislocation of the lens,vitreous cysticercosis,persistent hyperpllasia primary vitreous,etc.286(20. 50%)cataract eyes were examined and the power of intraocular...

The ultrasonic diagnosis of 1227 eye patients(1395 eyes)were reported.Among them,intraocular foreign bodies 20.29%,vitreous hemorrhage and opacity 15.56%,retinal detachment 12.76%,proliferative retinopathy 10. 25%,aphakia 8.24%,retinoblastoma 3.15%, ocular atrophy 2.80%.Rare disease of the eye included:scleral staphyloma,retrolental fibroplasia, dislocation of the lens,vitreous cysticercosis,persistent hyperpllasia primary vitreous,etc.286(20. 50%)cataract eyes were examined and the power of intraocular lens(IOLs)were calculated by SRK- Ⅱ formulum.The average value of the power is 18.01±3.72D.The correlation of age,sex and the incidence of the eye diseases were analytised.The clinical application of SRK-Ⅱ formulum and the ultrasonography of the rare eye diseases are also discribed.

本文对1227例共1395只眼的 B 型超声诊断进行分析。其中眼内异物占20.29%;玻璃体积血15.56%;视网膜脱离12.76%;玻璃体机化膜形成10.25%;无晶体眼8.24%,视网膜母细胞瘤3.15%;眼球萎缩实变2.80%。较少见疾病有巩膜后葡萄肿、晶体后纤维增生、品状体脱位、玻璃体囊虫病、原始玻璃体残留组织增生症等。白内障术前计算人工晶体屈光力286例(20.50,6),用 SRK-Ⅱ公式测算所需人工晶体屈光力平均值为+18.01D。分析了主要病种年龄、性别构成与临床发病特点的关系,并对 SRK-Ⅱ公式的实用价值及少见疾病的声象特征进行了讨论。

One hundred children patient,with leukocoria were examined by ultrasonography.The results showed retinoblastoma 61 cases ;Coats'disease 20 cases;persistance of primary vitreous body 5 cases;endophthalmitis 5 caa-es;retrolental fibroplasia 5 cases;retinal dysplasia 4cases. Based on these ultrasonic images,differential diagnosis was made and operative indication was proposed.Surgical effect and longtime follow-up observation confirmed the diagnosis accuracy rate being 99%.

对100例小儿白瞳孔患者施行了超声探查。结果:视网膜母细胞瘤61例(74只眼);Coats's病20例;原始玻璃体存留5例;眼内炎5例;晶体后纤维增生症5例;视网膜发育异常4例。根据声像图做出鉴别诊断并提出手术指征。手术和长期随访证实超声诊断准确率为99%。

 
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