vasculitis
And do an M.R.A.For vasculitis too.
|再用血管造影查查是不是脉管炎.
You guys thought it was vasculitis?
|你们还以为是脉管炎?
Adhesion Molecule Expression in Cutaneous Vasculitis.
某些粘附分子在皮肤血管炎中表达的研究。
Thus, a vasculitis is present.
在正下方是一个正常的肾小球。
Wegener's granulomatosis is a necrotizing vasculitis.
摘要韦格纳氏肉芽肿是一种坏死性血管炎。
This results from vasculitis.
脉管炎导致了此结果。
No other systemic signs of inflammation.Probably not vasculitis.
|没有其他发炎迹象. 应该不是血管.
The causes for hemoptysis include infection, cardiovascular disease, cancer, and vasculitis.
引起咳血的原因，包括有感染，心脏血管疾病，肿瘤，以及血管炎等。
For instance, instead of steroid for vasculitis, anticoagulant is used for APS.
是否能及时诊断并治疗、预防栓塞的复发，对病患的预后有重大的影响。
Conclusions PAN is a rare systemic vasculitis with complex clinical features.
结论结节性多动脉炎是一种少见的系统性血管炎,临床表现多种多样,容易误诊。
Serologic evidence of a systemic vasculitis was present in 50% of patients.
50%的患者有系统性脉管炎的血清学表现。
Juvenile gangrenous vasculitis of the scrotum: Is it a variant of pyoderma gangrenosum?
青少年阴囊坏疽性血管炎:坏疽性脓皮病的一种变异型?
HSP is a systematic small vasculitis which takes the small vasculitis as the main pathological change.
过敏性紫癜(HSP)是以无菌性小血管炎为主要病变的全身性血管变态反应性出血性疾病。
This muscular artery demonstrates vasculitis with chronic inflammatory cell infiltrates.
肌性动脉有慢性炎性细胞浸润的血管炎存在。
The secondary renal diseases included vasculitis,microangiopathy and cast nephropathy.
表现为 ARF最常见的继发性肾脏疾病是血管炎、微血管病及管型肾病。
There was no evidence of tumor, vasculitis or aneurysm from abdominal angiography and computed tomography.
在血管摄影及电脑断层中，并没有发现病人有腹内肿瘤、血管炎或血管瘤。
Vasculitis include s a group of diseases that have different patho-genesis and protean clinical manifesta-tions.
血管炎是一组发病机制各异,临床表现多样的疾病的总称。
Leucocytoclastic vasculitis is an immune-mediated, neutrophil-induced small vessel disease.
破白细胞性血管炎是一种免疫介导的中性粒细胞诱发的小血管病。
A skin biopsy showed leukocytoclastic vasculitis, indicating Henoch-Sch?nlein purpura (HSP).
皮肤的活组织检查示白细胞碎裂性血管炎，符合过敏性紫癜(HSP)。
The management of retinal vasculitis depends on the stage of the disease,inclu...
就此病的定义、病因、分类、基础研究、诊断及治疗等方面的最新进展进行综述。
The donor in the study had a history of homelessness and alcohol use and was hospitalized for cerebral vasculitis.
这项研究中的捐赠者有无家可归与酗酒的病史，且因为大脑血管炎住院；
Necropsies in dogs that die from the disease reveal severe hemorrhagic pneumonia and evidence of vasculitis.
死于犬流感犬只的尸检显示，犬流感能引起严重的失血性肺炎和血管炎。
Objective To analyze the clinical and histopathological features of urticarial vasculitis (UV).
摘要目的探讨荨麻疹性血管炎(UV)的临床和组织病理特征。
They all had multi-system involvement clinically and granulomatous vasculitis in pathology.
静止期炎症为肉芽组织所取代或有纤维化。
Kawasaki disease (KD) is an acute vasculitis of childhood, manifested by fever and signs of mucocutaneous inflammation.
川崎病（Kawasaki Disease KD）是一种以全身性血管炎为主要病变的儿童急性发热出疹性疾病。
Henoch-Schonlein purpura (HSP) is a systemic vasculitis of unknown cause and abdominal pain is usually complained.
摘要类过敏性紫斑症为一种不明原因的全身性血管炎，腹痛为其最常见的肠胃并发症；
Objective To evaluate the role of histopathologic examine in Cutaneous vasculitis.
目的：评价组织病理学在血管炎诊断中的价值。
Objective: To investigate the association of erythema nodosum、nodular vasculitis and mycobacterium tuberculosis.
目的:探讨结节性红斑、结节性血管炎和结核杆菌的关系。
The laboratory examinations related to leukocytoclastic vasculitis were within the normal limit.
其他和白血球破碎性血管炎相关的实验室检查结果均在正常范围。
Six patients were diagnosed to be suffering from vasculitis via lung or renal biopsy.
其中6例患者进行肾脏或肺活组织检查证实为血管炎。
Often, vasculitis is a feature of an autoimmune disease, such as systemic lupus erythematosus as was present in this patient.
通常，血管炎是自身免疫性疾病的特征性表现，如本例病人就患有系统性红斑狼疮。
Conclusion. Leptospirosis may have caused gut mucosal vasculitis, allowing salmonella to enter the bloodstream and infect the spine.
结论：钩端螺旋体病可能导致了内脏的粘膜血管炎，使沙门氏菌进入血流，感染脊柱。
Juvenile gangrenous vasculitis of the scrotum: Is it a variant of pyoderma gangrenosum? Caputo R. Marzano A.V. Di Benedetto A.
青少年阴囊坏疽性血管炎:坏疽性脓皮病的一种变异型?
Objective To study the expression and significance of cell adhesion molecules(ICAM 1,VCAM 1,ELAM 1) in cutaneous vasculitis.
目的 研究某些细胞粘附分子 (ICAM 1,VCAM 1,ELAM 1)在皮肤血管炎中的表达及其意义。
Methods PTCB was performed in 8 patients with WG,according to the clinical data of patients,Birmingham vasculitis activity score(BVAS) was calculated.
方法 8例经PTCB行病理组织学检查WG病人,根据其临床资料作BVAS评分,其结果与病理对照研究。
Histopathological examination for the resected specimen revealed cytomegalovirus infection with vasculitis and ischemic colitis.
病理报告显示检体呈巨细胞感染造成血管栓塞及缺血性坏死。
Results The eye sympotoms and uveitis of all patients were very mild, and their retinal vasculitis and retinal necrosis progressed slowly.
结果 所有患者发病时眼部症状及葡萄膜炎表现较轻，视网膜血管炎和坏死灶进展较慢。
Graft and patient survival rates among patients with ANCA-associated vasculitis are comparable to those observed in nondiabetic patients.
这些ANCA相关性血管炎患者的移植物和患者生存率与非糖尿病患者相当。
Zhao MH,Lockwood CM.ANCA defines clinical disease manifestations of vasculitis[J].Sarcoidosis Vasculitis Diffuse Lung Dis,1996,13:221.
姜筠赵明辉.原发性小血管炎肺脏受累[J].中华肾脏病杂志,:.
In patients with polymyositis and dermatomyositis, acute abdomen is attributed to intestinal vasculitis causing ischemia, ulceration or perforation.
在多发性肌炎和皮肌炎的病人中，急性腹痛症多是因为肠血管炎造成缺血。溃疡甚至穿孔而引起。
This article will take the intermediate uveitis, retinal vasculitis and intraocular lymphoma as examples to discuss in detail.
本文将结合中间葡萄膜炎，视网膜血管炎和眼内淋巴瘤病例进行分析讨论。
Leptospirosis is an infectious disease caused by a spirochaete. Symptoms include liver and kidney failure and vasculitis.
钩端螺旋体病是一种由螺旋菌引起的传染病。症状有肝脏、省脏衰竭和血管炎。
Method A systematic contrast study was performed on 180 patients with cutaneous vasculitis diagnosed by histopathologic examine.
方法：本文对180例经组织病理诊断为皮肤血管炎的病例，进行系统的对照分析。
At higher magnification, vasculitis with arterial wall necrosis is seen.Note the fragmented remains of neutrophilic nuclei (karyorrhexis).
高倍镜下，脉管炎患者动脉壁坏死，可见嗜中性粒细胞核碎片(核碎裂)。
IVIg might be an alternative treatment for some forms of systemic vasculitis with persistent disease activity after standard therapy.
静脉注射免疫球蛋白可以作为对某些经过标准治疗后仍然有着持续性疾病活动的系统性血管炎病人的一种替代疗法。
Vasculitis, as seen in Raynaud disease , or vasospasm, as seen in decompression sickness, may interfere with extraosseous circulation.
血管炎，看到的雷诺氏病，或血管痉挛，看到的减压病，可能会干扰外流通。
Objective To investigate the clinical significance of anti-PR3, anti-MPO antibody and ANCA in patients with systemic vasculitis.
目的探讨抗蛋白酶-3(PR3)抗体、抗髓过氧化物酶(MPO)抗体和抗中性粒细胞胞质抗体(ANCA),在系统性血管炎患者中的检测及临床意义。
Methods Make a definite diagnosis of , summarize and analyze to 20 for ANCA associated systemic vasculitis inflammation clinical materials of patient.
方法对20例确诊为ANCA相关性小血管炎患者的临床资料进行总结分析。
When the immunological vasculitis was confirmed, Most patients should be treated with a combination of immunosuppressive medications.
对自身免疫性血管炎的治疗首选联合应用皮质激素和环磷酰胺。
In four patients with vasculitis,whole-body MRA depicted luminal irregularity,narrowing or occlusion,aneurysm,and collateral circulation involving multiple vascular segments.
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