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纤维瘤
相关语句
  fibroma
    Non-ossifying Fibroma of Long Bone in Children
    儿童长骨非骨化性纤维瘤
短句来源
    There were 11 cases of non-ossifying fibroma, 7 cases of osteoid osteoma, 2 cases of bone cyst and 2 cases of fibrous dysplasia.
    其中非骨化性纤维瘤 11例 ,骨样骨瘤 7例 ,骨囊肿 2例 ,纤维异样增殖症 2例。
短句来源
    Diagnosis and treatment of nonossifying fibroma in children
    小儿非骨化性纤维瘤的临床特点及诊治
短句来源
    Objective: To study the characteristics, diagnosis, treatment and prognosis of non-ossifying fibroma of the long bone in children.
    目的:探讨儿童长骨非骨化性纤维瘤的临床特点、诊治方法及预后。
短句来源
    Methods: Six children (male 2, female 4, mean age 10.1 years) with nonossifying fibroma of long bone were admitted from 1988 to 1997. Of them, the solitary lesion in 4 cases were located in tibia, and the rest were multiple lesions.
    方法:总结1988~1997年收治发生在长骨的非骨化性纤维瘤6例。 其中男2例,女4例,平均年龄10.1岁。
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  “纤维瘤”译为未确定词的双语例句
    MRI as an important diagnostic method is especially emphasized here. Result: Lipoma and lipofibroma was 48%, Dermoid cyst and teratoma was 22%, Arachonoid cyst 15.6% , Neurofibroma 4%.
    脂肪瘤及脂肪纤维瘤占 48% ,皮样囊肿及畸胎瘤占 2 2 % ,蛛网膜囊肿占 15 .6% ,神经纤维瘤占 4%。
短句来源
    Mesenteric fibromatosis in a young girl without familial adenomatous polyposis
    1例家族性腺瘤性息肉病家族史阴性的年轻女孩患有肠系膜纤维瘤
短句来源
    Methods Longitudinal incision,excised the hamartomatous tissue、scar tissue、proliferated periosteum.
    方法 本组共 9例 ,做骨不连处纵切口 ,切除骨不连处瘢痕、纤维瘤样组织、硬化骨、部分增厚的骨膜。
短句来源
    To investigate the diagnosis,treatment and the features of breast giant fibroadenomas in children.
    [目的]探讨小儿乳腺巨纤维瘤的特点和恰当的诊治方法。
短句来源
    Six cases with breast giant fibroadenomas were treated in our hospital between 1983 and 2000.The clinical profile,pathologic characteristic and prognosis were analyzed.
    [方法]从1983年~2000年共收治6例乳腺巨纤维瘤患儿 ,分析其临床表现、病理学特点和预后。
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  fibroma
The structure of these tumorlike formations is characteristic of fibroma.
      
An unusual sphenoid ridge tumor: Cementifying fibroma
      
Value of dynamic enhanced MR imaging for the differential diagnosis between ovarian fibroma and subserosal leiomyoma
      
These included hemangiomas and metastatic cancer (previously identified in dinosaurs), desmoplastic fibroma, and osteoblastoma.
      
CT and MRI of congenital sinonasal ossifying fibroma
      
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Thirteen patients with neurofibromatosis from three families are reported, it including 9 males and 4 females from 7 to 66 years old. Three families were investigated and the disease in terms of etiology, pathology, diagnosis, treatment and prognosis are discussed.

本文报告三个不同家系神经纤维瘤病患者共13例。其中男性9例,女性4例;最小7岁,最大66岁;并作了三个家系调查。并对本病的病因、病理、诊断、治疗与预后等方面进行了讨论。

Objective: To study the characteristics, diagnosis, treatment and prognosis of non-ossifying fibroma of the long bone in children. Methods: Six children (male 2, female 4, mean age 10.1 years) with nonossifying fibroma of long bone were admitted from 1988 to 1997. Of them, the solitary lesion in 4 cases were located in tibia, and the rest were multiple lesions. All cases underwent operation including curettage of foci and iliac autotransplantation, or segmental resection and free vascularized fibula transplantation....

Objective: To study the characteristics, diagnosis, treatment and prognosis of non-ossifying fibroma of the long bone in children. Methods: Six children (male 2, female 4, mean age 10.1 years) with nonossifying fibroma of long bone were admitted from 1988 to 1997. Of them, the solitary lesion in 4 cases were located in tibia, and the rest were multiple lesions. All cases underwent operation including curettage of foci and iliac autotransplantation, or segmental resection and free vascularized fibula transplantation. The diagnosis was confirmed histologically. The followup was 8 years and 7 months without recurrence. Conclusions: The cause of nonossifying fibroma is uncertain, it may be a benign tumor originated from the osseofibrous. It should be differentiated from osteofibrous dysplasia, giant cell tumor, single bony cyst etc. The advantage of curettage of foci and autogenous bone grafting are rapid bony healing and early weight carrying.

目的:探讨儿童长骨非骨化性纤维瘤的临床特点、诊治方法及预后。方法:总结1988~1997年收治发生在长骨的非骨化性纤维瘤6例。其中男2例,女4例,平均年龄10.1岁。单发病灶在胫骨4例;多发性2例,同时发生在胫、腓骨1例,胫骨、腓骨及双侧股骨同时4处受累1例。6例均行手术治疗,包括单纯刮除加植骨和瘤段切除加游离腓骨移植。结果:6例均病理证实为非骨化性纤维瘤。随诊最长8年7个月,无一例复发。结论:该瘤病因尚不明确,可能为生发在骨内纤维组织的良性肿瘤。临床上应与纤维性皮质骨缺陷、骨纤维结构不良、骨巨细胞瘤、单发性骨囊肿等相鉴别。对较大病灶,在瘤灶刮除后采用带血管腓骨移植或带血管蒂腓骨移位植骨的治疗方法,具有骨愈合过程快、患骨可及早负重的优点。

Purpose To investigate the characters of diagnosis and treatment modality for malignant schwannoma in children.Methods Elevenchildren cases with malignant schwannoma were treated in our institute beween June 1988 and October 1997.The clinical and pathological features,themethods of diagnosis and treatments,and the follow-up results were analyzed retrospectively.Results The tumor was located in cervical region in 3cases,in region of scapular in 1 case,in mediastinum in 1 case and in abdomen in 6 case. 3 cases...

Purpose To investigate the characters of diagnosis and treatment modality for malignant schwannoma in children.Methods Elevenchildren cases with malignant schwannoma were treated in our institute beween June 1988 and October 1997.The clinical and pathological features,themethods of diagnosis and treatments,and the follow-up results were analyzed retrospectively.Results The tumor was located in cervical region in 3cases,in region of scapular in 1 case,in mediastinum in 1 case and in abdomen in 6 case. 3 cases had coexistent von Recklinghausen's diseaes. Allof the 11 cases underwent surgical treatment.Some of them were treated by combination withe adjuvant chemotherapy ofr ra diotherapy.At the time of thelast follow-up,10 patients had died of local invasion of metasis of the tumor,only one continued to be tumor free for 14 months after operation.conclusions The clinical manifestations and pathological features of malignant schwannoma in children are different from that of in adults.The adjuvantchemothersapy and radiotherapy have some effects,but the prognosis is still very poor.The satisfactory treament results depend on early diagnosis,radical openative resection and proper conbined postoperative management.

(目的)探讨小儿恶性雪旺氏细胞瘤的发病特点及诊治方法。(方法)分析1988年6月至1997年10月收治的11例小儿恶性雪旺氏细胞瘤病例的临床病理特征、诊治方法及预后。(结果)颈部3例,腹部6例,纵隔及肩胛后各1例。其中3例为神经纤维瘤病变。均手术治疗,部分病例会并化、放疗。仅1例术后无瘤生存14个月,其余均在术后1-15个月死于肿瘤转移、局部浸润及相关并发症。(结论)小儿恶性雪旺氏细胞瘤发病不同于成人。辅助化、放疗有一定疗效,但预后不佳,迫切需要寻找新的综合治疗方法。

 
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