神经鞘炎

基本解释 (translations)

neurilemmitis  ·  neurothecitis  ·  schwannitis

词组短语

adventitial neuritis

与神经鞘炎相关的网络例句 [注：此内容来源于网络，仅供参考]

Those with heterogeneous enhancement were often of acquired etiology, such as ranula, lymphoma, neurilemmoma, parotid adenoma, metastatic nodes and tubercubus adenitis, etc.

至於那些有异质性加强的病变，通常属於后天性疾病，例如：舌下囊肿、淋巴瘤、神经鞘瘤、腮腺瘤、转移性淋巴结、结核性淋巴腺炎等。

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。

The notable proliferation was not observed by eyes in the local of injection. The infiltration of inflammation cells and mild proliferation of fibrocyte around dura mater was observed by HE stained in 4 and 8 weeks after injection. Infiltration and exudation of inflammation cells was observed by HE stained in epidural nerve root. Compared with group A, no changes of group B, C and D were observed under specific stained. Proliferation of type Ⅱ collagen fibers around dura mater was seen under immunohistochemical stained in 4 and 8 weeks after injection. There is no significant demyelination changes under LFB stained. The thickness and shape of the myelin sheath in epidural nerve root was not regular under transmission electronic microscopy in 4 and 8 weeks after injection. Fibroblast was also seen there. In nerve endometrium, macrophage could be seen under TEM, myelinated nerve fiber changed significantly, but nonmyelinated nerve fiber changed mildly. When 8 weeks, the changes of group D is smaller than the group B and C.

给药局部肉眼观察未见明显的纤维组织增生；HE染色可见B、C、D三组给药后四周及八周时硬膜内外均有炎细胞浸润，纤维细胞轻度增生，硬膜外神经根内有炎细胞浸润及炎性渗出；特殊染色B、C、D三组同A组相比未见有脊髓及神经根的改变；免疫组化染色，给药后四周及八周时，硬膜内外均有Ⅱ型胶原纤维增生；固兰染色B、C、D三组未见有明显脱髓鞘改变，与A组相比无明显异常改变；电镜观察B、C、D三组在给药后的四周及八周时，表现为硬膜外神经根内髓鞘厚薄不一，形状不规则，可见成纤维细胞，神经内膜中可见有巨噬细胞；粗大的有髓神经纤维变化明显，无髓神经纤维受累较轻；八周时电镜下D组改变较B、C两组为轻。

It was considered an effective and ideal model of PM.2 uPA,PAI-1 and TNF-αwere all involved in the pathogenesis of PM and participated in the process of the degeneration,apoptosis and necrosis of the diseased muscle.3 MMP-9 and TIMP-2 immunoreactivity were positive in the capillary,venous wall,arteriola endotheliocyte and neurilemma in the normal group skeletal muscle,but more intensive in EAM.They may aggravate the pathological changes of the muscle in human PM.

结论1兔纯化的肌球蛋白加含卡介苗的完全弗氏佐剂可仿制出人类多发性肌炎的理想动物模型。2 UPA、PAI-1和TNF-α参与多发性肌炎的肌纤维坏变过程。3 MMP-9和TIMP-2在正常肌肉组织中的毛细血管、静脉管壁、动脉肉皮细胞和神经鞘膜表达，在多发性肌炎中，参与加重肌纤维的坏变过程。

"Myelin basic protein as an encephalitogen in encephalomyelitis and polyneuritis following rabies vaccination".

髓鞘碱性蛋白作为encephalitogen在脑脊髓炎和多发性神经炎后狂犬病疫苗接种。

There were infiltration of inflammatory cells inside nerve tissue and perivascular cuffings in HE staining. In trichrome staining, the axon with inhomogeneous chromatosis was swollen and beaded-discontinued; The myelin was porous and partly disaggregated.

HE染色发现神经组织内炎细胞浸润，血管&袖套&样病灶形成；三色染色可见轴突肿胀，呈串珠状，且不连续，着色不均匀；髓鞘结构层次紊乱，疏松，崩解。

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。

与神经鞘炎相关的网络解释 [注：此内容来源于网络，仅供参考]

multiple sclerosis：多发性硬化症

(三)多发性硬化症(multiple sclerosis)是一种青、壮年时期的中枢神经系统脱髓鞘疾病,其特点为病灶播散在病程中常有缓解和复发的反复出现. 病损部位的不同,临床表现可多种多样. 常有精神症状的言语障碍. 颅神经功能障碍以球后神经炎为首发症状多见.

retrobulbar neuritis：球后视神经炎

球后视神经炎(Retrobulbar neuritis)一般分为急性和慢性两类,以后者较多见. 由于视神经受侵犯的部位不同,球后视神经为可分许多不同类型:病变最常侵犯视盘黄斑束纤维,因该束纤维在球后眶内段视神经中央部分,故又名轴性神经炎;当病变由神经鞘膜侵犯视神

spinal arachnoiditis：脊髓蛛网膜炎

(七)脊髓蛛网膜炎(spinal arachnoiditis)起病可急可缓,可因感染、外伤、药物鞘内注射,脊髓或脊椎病变等继发. 可先有发热或感冒等症状,随后出现神经根性疼痛与脊髓压迫症状,表现为截瘫或四肢瘫,同时有感障碍与括约肌功能障碍. 本病常有特征性的多个病灶的表现;

medullitis：骨髓炎,脊髓炎

\\"髓形成,髓鞘形成\\",\\"medullation\\" | \\"骨髓炎,脊髓炎\\",\\"medullitis\\" | \\"神经管胚细胞瘤\\",\\"medultoblastoma\\"

neurilemmitis：神经鞘炎

neurilemmalcell 神经膜细胞 | neurilemmitis 神经鞘炎 | neurilemmomaofbone 骨神经鞘瘤

neurinoma：神经瘤

neurilemmoma 神经鞘瘤 | neurinoma 神经瘤 | neuritis 神经炎

neuromyelitis optica：视神经脊髓炎

(一)视神经脊髓炎(neuromyelitis optica)是合并有视神经和脊髓的脱髓鞘疾病. 20~40岁好发,脊髓与神经症状常先后(或后先)出现,脊髓病变胸段最多,多呈横贯性病征,此外可有阵发性剧烈抽搐,或有烧灼样的局部痛性强直性痉挛发作. 视神经为视乳头炎或球后视神经炎,

retinal periphlebitis：視網膜靜脈周圍炎

视网膜静脉周围炎(retinal periphlebitis)又称Eales病或青年性复发性视网膜玻璃体出血,多发生于男性青壮年,双眼可同时发病或先后发病,有复发趋势. 青年人突发性或反复发作性视网膜或玻璃体出血,而无视神经乳头水肿. 病变视网膜静脉周围伴随有白鞘,