- 更多网络例句与纤维性肌炎相关的网络例句 [注：此内容来源于网络，仅供参考]
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Results: All rats in experiment group devloped CAG at the end of 12 weeks with the following Pathological changes of CAG such as thin mucosa layer, thick muscle layer, decreased glandes, soakaging inflammation cells in microscope and with the time prolonging, the atrophy of gastric mucosa became more serious; In normal control group and normal feeding group, the IL-6 and IL-8 content in blood serum are the same at every time point; In experiment group, IL-6 became increased from 4wk and kept high level from 4wk to l2wk and had significant difference compared with normal controls.
结果：灌胃至12wk时出现胃粘膜层变薄，固有层腺体减少，固有层纤维结缔组织增生，粘膜肌层明显增生，慢性炎细胞浸润等萎缩性胃炎表现，随著热盐水灌胃时间的延长，32wk胃粘膜萎缩程度明显加重；正常对照组和正常餵养组大鼠各时间点血清IL-6，IL-8含量基本相同。
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Clinical diagnostic considerations ranged from benign entities such as rhabdomyoma, intramuscular lipoma, fibromatosis, myositis ossificans, proliferative myositis, inflammatory myofibroblastic tumor, and inflammatory myopathy to malignant entities such as rhabdomyosarcoma, leiomyosarcoma, liposarcoma, and lymphoma.
这些病例的临床考虑多样，有良性的横纹肌瘤、肌内脂肪瘤、纤维瘤病、骨化性肌炎、增生性肌炎、炎性肌纤维母细胞瘤和炎性肌病，也有恶性的横纹肌肉瘤、平滑肌肉瘤、脂肪肉瘤和淋巴瘤。
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Methods:Percutaneous transluminal renal angioplasty with stent was performed on 203 consecutive patients with severe renal artery stenosis, caused by atheroma (123),arteritis (62) and fibromuscular displasia (18),for poorly controlled hypertension or preservation of renal function,who subsequently underwent 6 -month clinical follow-up for the effect of the procedure on renal f...
1999年至2004年，我院连续203例肾动脉严重狭窄的患者，其中男性128例(63.1％)，女性75例(36.9％)，年龄13-82(54±18)岁，病因分别为动脉粥样硬化123例(60.6％)、大动脉炎62例(30.5％)和纤维肌性结构不良18 例(8.9％)，因严重高血压或伴有肾功能不全而进行了肾动脉支架置放术，并随诊6个月，观察手术对患者血压、肾功能的影响。
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While symptoms may seem to improve almost immediately after surgery, it takes approximately 6-12 months before new vessels develop sufficiently. Diseases associated with moyamoya include sickle cell anemia, atherosclerosis, prior radiation therapy to the skull base in children, and less commonly neurofibromatosis, tuberous sclerosis, meningitis, retinitis pigmentosa, fibromuscular dysplasia, Down's syndrome and Fanconi's anemia.
手术之后几乎立即可以看到症状的好转，新的血供充分发展起来大概要花6-12月时间。moyamoya相关的疾病包括镰状细胞性贫血、动脉粥样硬化、颅底部放疗，不太常见的有神经纤维瘤病，结节性硬化、脑膜炎、色素性视网膜炎、纤维性肌发育不良、Down氏综合症和Fanconi's 贫血症
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It is known that cardiovascular risk factors, smoking, fibromuscular dysplasia, or moyamoya disease are frequently found as an aetiological factor in patients with bilateral ICA occlusion, whereas essential thrombocytaemia, giant cell arteritis, and BD are among the very rare causes.
众所周知，双侧颈内动脉闭塞的常见病因为心血管危险因素、吸烟、纤维肌性发育不良、Moyamoya病/烟雾病/脑底异常血管网病等，而特发性血小板增多症（essential thrombocytaemia， essential thrombocythemia， ET）、巨细胞性动脉炎、白塞病则为非常罕见的原因。
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Resujts:① The distribution of lesions are mostly symmetrical, extensive, predominant in the middle and lower lung fields, and posterior areas in peripheral;② There are so many HRCT findings of lung, ILD is predominant: intralobular interstitial thickening 46 cases (100%), ground-glass opacity 41 cases (89.13%), peribronchovascular or centrilobular interstitial thickening 40 cases (86.96%), interlobular septal thickening 38 cases (82.61%), irregular linear opacity 37 cases (80.43%), small nodular opacity 34 cases (73.91%), subpleural line 27 cases (58.70%), bmnchiectasis or bronchiolectasis 19 cases (41.30%), patch opacity 18 cases (39.13%), expiratory mosaic sign 15 cases (32.61%), interface sign 14 cases (30.43%), honeycombing 12 cases (26.09%), emphysema or bulla 3 cases, cystic airspace suspected 1 case, and atelectasis suspected 1 case;③ Mediastinum and pleura: multiple small lymphonodi in mediastinum 41 cases (89.13%), pleural thickening or rough 38 cases (82.61%), esophagoectasis 11 cases (23.91%), unilateral little pleural fluid 1 case, and mediastinal emphysema 1 case.
结果：①皮肌炎肺部病变分布呈对称、广泛、偏中下、偏外后的特点；②肺部HRCT表现多样，以肺间质性改变为主：小叶内间质增厚46例(100%)，磨玻璃影41例(89.13%)，支气管血管束增宽或小叶核心增大40例(86.96%)，小叶间隔增厚38例(82.61%)，不规则纤维索条影37例(80.43%)，结节影34例(73.91%)，胸膜下线27例(58.70%)，支气管或细支气管扩张19例(41.30%)，斑片影18例(39.13%)，呼气相马赛克征15例(32.61%)，界面征14例(30.43%)，蜂窝影12例(26.09%)，肺气肿或肺大泡3例，单纯囊状气腔1例，肺不张l例；③纵隔及胸膜：纵隔小淋巴结影41例(89.13%)，胸膜增厚或毛糙38例(82.61%)，食管扩张11例(23.91%)，单侧少量性胸腔积液1例，纵隔气肿1例。
- 更多网络解释与纤维性肌炎相关的网络解释 [注：此内容来源于网络，仅供参考]
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intestinal metaplasia：肠上皮化生
(2)肠上皮化生(intestinal metaplasia) 这种化生常见于胃体和/或胃窦部. 肠上皮化生常见于慢性萎缩性胃炎、胃溃疡及胃粘膜糜烂后粘膜再生时. 结缔组织化生也比较多见. 多半由纤维结缔组织化生为骨、软骨或脂肪组织. 如骨化性肌炎(myositis ossificans)时,
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fibromuscular hyperplasia：纤维肌性增生
fibromuscular dysplasia 肌纤维发育不良 | fibromuscular hyperplasia 纤维肌性增生 | fibromyositis 纤维性肌炎
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fibromyectomy：纤维肌瘤切除术
fibromuscular 纤维肌性的 | fibromyectomy 纤维肌瘤切除术 | fibromyitis 纤维性肌炎
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fibromyitis：纤维性肌炎
fibromyectomy 纤维肌瘤切除术 | fibromyitis 纤维性肌炎 | fibromyomainomyoma 纤维肌瘤
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fibromyositis：纤维性肌炎
fibromuscular hyperplasia 纤维肌性增生 | fibromyositis 纤维性肌炎 | fibrosis 纤维化
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myositis ossificans：骨化性肌炎
骨化性肌炎(myositis ossificans)是一种以纤维性、软骨或骨性化生为特征的局部反应性病变. 常发生于靠近骨或骨膜的软组织. 骨化性肌炎一词不恰当,因为骨骼肌并不受累也无炎症改变. 病因不同可分为创伤性骨化性肌炎与进行性骨化性肌炎.