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There were 36 males and 40 females,with the average age of 47.7 years.36 patients presented with sciatica and perineal numbness,11 patients had painless mass and the other 20 were identified due to other causes.Among 67 benign neurogenic tumors,54 were originated from S1-S3 nerves,3 from S4-S5 nerves and 11 from the presacral space without caudal involvement.Giant cell tumor was found in 60 patients,which included 24 males and 36 females,with an average age of 32 years.Upper sacrum(S1-S2) was involved firstly.There were 56 patients(average,37.7 years) diagnosed as other primary benign bone tumors,which included 24 cases of teratomas,epidermoid cyst or dermoid cyst.Other malignant tumors,including chondrosarcoma (17),Ewing′s sarcoma/PNET(14),multiple myeloma(12),lymphoma(6) and osteosarcoma(6) were found in 64 patients.

其中脊索瘤95例,男62例,女33例,平均年龄55.7岁,骶尾区疼痛是主要症状(82例),半数以上患者伴有坐骨神经痛,肿瘤多先累及低位骶骨(S3~S5);神经源性肿瘤76例,男36例,女40例,平均年龄47.7岁,神经纤维瘤43例,神经鞘瘤24例,恶性神经鞘瘤9例,主诉多为坐骨神经痛、会阴部麻木(36例)和无痛性包块(11例),20例患者为查体或其他原因检查时发现,67例骶骨良性神经源性肿瘤起源于S3以上神经者54例,起源于S3以下神经者3例,发生于骶前未累及骶管者10例;骨巨细胞瘤60例,男24例,女36例,平均年龄32岁,腰骶尾部不适(37例)、坐骨神经痛(21例)是主要的临床表现,肿瘤多先累及上位骶骨(S1~S2);骶骨其他原发良性肿瘤及瘤样病变56例,包括畸胎瘤、皮样囊肿、表皮样囊肿共24例;其他原发恶性肿瘤64例,包括软骨肉瘤17例,尤文肉瘤14例,多发性骨髓瘤12例,成骨肉瘤6例等。

The time of hight incidence of gout, tuberculosis and traumatic arthritis is from 20 to 40 years old; peak age of rheumatoid arthritis is 40 to 60 years of age; and synovial chondromatosis, osteoarthritis, infectious arthritis lumbar hip disease caused the incidence of knee pain increases with age increased.

3痛风、结核及创伤性关节炎的高发年龄为20~40岁,类风湿性关节炎的高峰年龄为40~60岁,滑膜软骨瘤、骨性关节炎、感染性关节炎及腰髋部疾病造成膝关节疼痛的发病率随年龄的增长而升高。

We report the case of a patient who had infrapatellar bursal osteochondromatosis in association with unresoled Osgood-Schlatter disease.

我们的报道是一例伴有未缓解的Osgood-Schlatter病的髌骨下粘液性骨软骨瘤病的患者。

In summary, we report an unusual case of infrapatellar bursal chondromatosis associated with an unresoled Osgood- Schlatter lesion.

综上所述,我们报道了一个罕见的与未缓解的Osgood-Schlatter损害相关的髌骨下粘液囊骨软骨瘤病病例。

In addition, the present case is unique in that the bursal chondromatosis lesion deeloped in association with a large, unresoled Osgood-Schlatter lesion.

而且,本例粘液囊骨软骨瘤病损害的发生与一个大的、未缓解的Osgood-Schlatter损害相关,这还是绝无仅有。

Therefore, our data show that in cases when clear cell chondrosarcoma and chondroblastoma pose a diagnostic challenge, the presence of type II collagen in the extracellular tumour matrix significantly supports the diagnosis of clear cell chondrosarcoma and aids in distinguishing it from chondroblastoma.

我们的数据表明,在诊断透明细胞软骨肉瘤和成软骨细胞瘤受阻时,细胞外肿瘤基质中II型胶原的存在对于诊断透明细胞软骨肉瘤相当有帮助,并有助于和成软骨细胞瘤间的鉴别。

Focus on research work and clinical studies in musculoskeletal oncology, especially about mechanism and biological therapy of osteosarcoma, such as proteomics studies of osteosarcoma, prospective control study of osteosarcoma, registration system of musculoskeletal oncology and genic tests about the familial inheritance osteoenchondroma, etc.

拟开展《骨肉瘤特异性相关抗原的蛋白质组学研究》、《骨肉瘤多中心前瞻性随机对照研究》、《骨与软组织肿瘤注册-会诊-随访登记系统》、《多发性骨软骨瘤家族遗传性基因的检测》等课题的相关研究工作,承担国家、省级和市级重大项目等课题的申报。

Methods X-ray,CT and MRI findings in 14 cases with synovial osteochondromatosis were analyzed retrospectively.

回顾性分析14例滑膜性骨软骨瘤病患者的X线、CT和MRI的影像学资料。

In the latest Mayo Clinic series of bone tumors published by Unni, sacral osteochondromas represented 3 of 748 reported osseous exostoses.

在最近一期Unni出版的Mayo骨肿瘤临床系列杂志中统计,骶骨骨软骨瘤只占748例骨外生骨疣中的3例。

Very rarely, features of high grade osteosarcoma, leiomyosarcoma, chondrosarcoma, rhabdomyosarcoma and malignant peripheral nerve sheath tumor are found.

罕见的情况下可以找见高级别骨肉瘤、平滑肌肉瘤、软骨肉瘤、横纹肌肉瘤和恶性外周神经鞘膜瘤的特征。

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