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        west china medical publishers
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        find Keyword "肉芽" 47 results
        • CLINICAL FEATURES AND THE CAUSES OF MISDIAGNOSIS OF GASTRIC EOSINOPHILIC GRANULOMA (A REPORT OF 14 CASES)

          目的 探討胃嗜酸性肉芽腫的診斷、誤診原因和治療方法。方法 對14例胃嗜酸性肉芽腫的臨床資料進行回顧性分析。結果 全部病例均有上腹疼痛和返酸史; 伴潰瘍形成11例,穿孔4例,上消化道出血3例; 術前行胃鏡檢查2例,X線鋇餐透視檢查6例,無1例獲確診; 其余病例亦全部誤診為胃潰瘍或癌腫。結論 胃鏡多部位取材,特別是在潰瘍與周邊粘膜移行處,采取挖掘式取材,能減少誤診率; 胃大部切除術是主要的治療方法。

          Release date:2016-09-08 01:59 Export PDF Favorites Scan
        • 變應性肉芽腫性血管炎二例報告并文獻復習

          目的 加深對變應性肉芽腫性血管炎(又稱Churg-Strauss綜合征,CSS)的認識,提高臨床診斷及治療水平,改善預后。方法 復習國內發表的臨床診斷為CSS的28例病例,結合近期南華大學第二附屬醫院收治的2例變應性肉芽腫性血管炎病例進行臨床分析。結果 30例患者中,男16例(53.3%),女14例(46.7%);年齡7~76歲,平均41.4歲。14例以喘息為首發癥狀,19例有支氣管哮喘癥狀,病變可累及呼吸系統(63.3%)、神經系統(36.7%)、皮膚(50.0%)、消化系統(33.3%)、心臟(13.3%)、腎臟(6.7%)、關節肌肉(3.0%)、外周血管(6.7%)及眼部(6.7%)等。28例(93.3%)存在嗜酸粒細胞異常,平均值為29.5%,6例患者抗中性粒細胞胞漿抗體核周型(P-ANCA)、抗中性粒細胞胞漿抗體胞漿型(C-ANCA)檢查均提示陽性。18例CSS患者肺部CT存在異常,多表現為浸潤性、磨玻璃樣、彌漫性間質樣或結節樣改變;14例取得病理學檢查依據,表現為嗜酸粒細胞浸潤,血管炎及血管外肉芽腫。臨床治療主要使用糖皮質激素和免疫抑制劑(如環磷酰胺),總體預后較好。結論 變應性肉芽腫性血管炎是一種罕見的系統性血管炎疾病,臨床表現缺乏特異性,易漏診、誤診,當患者表現為哮喘、外周血嗜酸粒細胞增多及肉芽腫性血管炎時,應高度警惕此病。

          Release date:2016-08-30 11:31 Export PDF Favorites Scan
        • 家族遺傳性多趾嵌趾甲致多發性肉芽腫一例

          Release date:2016-09-01 09:29 Export PDF Favorites Scan
        • A STUDY OF FIBROBLAST GROWTH FACTOR IMPROVING WOUND HEALING IN MOUSE SKIN

          Abstract To observe the effect of fibroblast growth factor (FGF) on wound healing, 50 mice were divided into 5 groups. On the back of every mouse, 2 wounds were made by operative cuts, one for experiment and the other for control. The wounds of the experimental group were covered with 0.5ml FGF solution (contented FGF 300 μg/ml, heparin 100 μg/ml), whereas the wounds of the control group were covered with 0.5ml 0.9% NaCl solution. All of the wounds were dressed by sterilized gauze, and received the same treatment once a day. After 1,3,5,7,10 days, the mice in every group were sacrificed and the tissues of the wounds were collected and prepared for microscopic examination. The results showed that the capillaries and fibroblasts in the experimental group were markedly increased and reached the peak 2~3 days earlier than those in the control group. It was suggested that FGF promoted the formation of granulation tissue and the wound healing.

          Release date:2016-09-01 11:10 Export PDF Favorites Scan
        • Clinical Characteristics and Renal Outcome in Elderly Patients with Antineutrophil Cytoplasmic Autoantibody Associated Vasculitis with Renal Involvement

          ObjectiveTo analyze the clinical characteristics and renal outcome of elderly patients with antineutrophil cytoplasmic autoantibody (ANCA) associated vasculitis (AAV) with renal involvement. MethodsWe retrospectively analyzed the clinical data of 147 patients with ANCA relate vasculitis treated between June 2006 and June 2012. Based on the age, the patients were divided into elderly group (65 years or older, n=50) and non-elderly group (younger than 65, n=97). The disease course, clinical characteristics, ANCA serological indexes, renal pathological change and prognosis of patients in the two groups were compared and studied. ResultsIn the elderly group, there were 3 cases of Wegener granulomatosis (WG), 45 of microscopic polyangiitis (MPA), and 2 of pauci-immune crescentic glomerulonephritis (PICGN). The non-elderly group had 8 cases of WG, 82 of MPA, 6 of PICGN, and 1 of allergic angitis granulomatosis. There were 5 cases of positive cANCA and 44 of positive pANCA in the elderly group. The elderly patients had significantly more pulmonary involvement than the younger patients (P=0.030). No significant difference was detected between the two groups in combined pulmonary infection (P=0.281) or combined infectious index C-reactive protein (P=0.326). Elderly patients were less likely to respond to sufficient treatment with pulse intravenous methylprednisolone therapy (P=0.035) and cyclophosphamide (P=0.043), and had worse renal outcome than younger patients (P=0.040). ConclusionElderly patients with AAV have more prevalent pulmonary involvement and have severe complication of pulmonary infection, which affects mortality and morbidity of ANCA-associated systemic vasculitis.

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        • GASTRIC EOSINOPHILIC GRANULOMA (A REPORT OF 22 CASES)

          To investigate the diagnosis, pathological characteristics and clinical treatment of gastric eosinophilic granuloma (GEG). Twenty two cases with GEG diagnosed by operation and pathology were analyzed. In this series 14 cases subjected to partial gastrectomy, 6 cases to subtotal gastrectomy, 1 case to total gastrectomy, and 1 case to radical gastrectomy. After 1-10 years of follow-up, 1 case, who was combined with gastric carcinoma at the first operation, died of the recurrence and extensive metastasis of gastric carcinoma on the 4th year after operation, 2 cases were reoperated on the 2nd or 6th year respectively after operation for forward complication, and the others recoverd well. The authors consider that gastrofiberscopic diagnosis is key to lessen the preoperative misdiagnosis, and the scope of dissection mainly depends on the size and type of focus. It is no need for extensive dissection.

          Release date:2016-08-29 09:18 Export PDF Favorites Scan
        • 肉芽腫性肺疾病

          肉芽腫性肺疾病( GLD) 或稱肺肉芽腫病( lung granulomatosis) , 是一組病因不同但以肉芽腫性炎癥和肉芽腫形成為共同病理特征的肺部疾病的總稱。所謂肉芽腫( granuloma) 是指巨噬細胞及其演化的細胞( 如上皮樣細胞、多核巨細胞) 聚集和增生所形成的境界清楚的結節狀病灶,是一種特殊類型的慢性增生性炎癥。肉芽腫的形成是機體對外來刺激的一種重要的防御機制, 其結果是致病因子被局限于肉芽腫內。肉芽腫不應與肉芽組織( granulation tissue)相混淆, 后者是由新生薄壁的毛細血管以及增生的成纖維細胞構成, 并伴有炎性細胞浸潤, 肉眼表現為鮮紅色, 顆粒狀,柔軟濕潤, 形似鮮嫩的肉芽故而得名, 為幼稚階段的纖維結締組織。肉芽腫性肺疾病并不是一種獨立的疾病, 病因較多, 治療上也存在很大差別, 因而如何確定其診斷極為重要。

          Release date:2016-09-13 04:06 Export PDF Favorites Scan
        • MRI Appearances of Xanthogranulomatous Cholecystitis in 7 Patients

          ObjectiveTo investigate clinical value of MRI examination in diagnosis of xanthogranulomatous cholecystitis (XGC), and to analyze pathologic correlation of various imaging findings. MethodsMRI imaging data of 7 patients with XGC proved by surgery and pathology who underwent entire MRI sequences examination in Sichuan Provincial People's Hospital from Jan. 2013 to Dec. 2015, were analyzed retrospectively. The thickness and contrast enhancement of gallbladder wall, gallbladder wall nodules, completeness of gallbladder mucosa lines, gallbladder stones, and the changes around the gallbladder were focused in every patient. ResultsIn 7 patients with XGC: gallbladder wall thickening occurred in all patients, in which 2 patients were local thickening, 5 patients were diffuse thickening; ‘hypodense band sign' was found by enhance scan in 4 patients; the multiple intramural nodules were presented in 5 patients, which were low signal intensity on T1WI image and high signal intensity on T2WI image; the mucosal lines were continuous in 6 patients and discontinuous in 1 patient; 6 patients combined with cholecystolithiasis. The fat layer around the gallbladder was found fuzz in 7 patients, liver and gallbladder boundaries were not clear in 7 patients; temporal enhancement of arterial phase in liver parenchyma was observed in all patients, and 1 patient combined with liver abscess. Hilar bile duct narrowed and intra-hepatic bile duct dilated in 2 patients, intra-hepatic and extra-hepatic bile duct slightly dilated in 2 patients (lower part of the choledochus stone was found in 1 patient), liver cyst was observed in 3 patients, single or double kidney cyst was observed in 4 patients; all patients were not found intraperitoneal or retroperitoneal swelling lymph nodes. ConclusionMRI examination can accurately describe various imaging features of XGC, so MRI has important value in diagnosis of XGC.

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        • DIAGNOSIS AND TREATMENT OF EOSINOPHILIC GRANULOMA OF LONG BONES IN CHILDREN

          Objective To investigate the operative procedure and the effectiveness of eosinophil ic granuloma (EG) of long bones in children. Methods Between January 2005 and December 2009, 14 patients with EG of long bones were treated. There were 9 boys and 5 girls, aged from 1 to 13 years (mean, 6.5 years). The locations were femur in 5 cases, humerus in 4 cases, tibia in 2 cases, fibula in 1 case, and femur compl icated with tibia in 2 cases. The disease duration was7 days to 10 months (median, 2 months). X-ray films showed that osteolytic destruction had clear boundary, which did notinvolve the epi physeal plate. Of 14 cases, 12 cases of tumor were treated by curettage, autologous il iac bone or combined artificial bone graft repair, and 2 cases were treated by resection, autologous il iac reconstruction, plate and screw fixation. Five cases compl icated with pathological fracture underwent reduction and fixation. Results All cases were diagnosed pathologically as having EG. All incisions healed by first intention. A total of 12 patients were followed up 1 to 4 years (mean, 2 years). The X-ray films showed tumor focus and pathological fracture healed within 3 to 4 months (mean, 3.5 months). Tibial lesion was found in 1 case of femoral tumor after 8 months, and was curred after reoperation. No recurrence occurred in other 11 cases. According to comprehensive assessing standard of X-ray film and joint function, the results of all cases were excellent. Conclusion EG of long bones in children is more common in the femur and humerus. Tumor curettage and autologous il iac bone graft repair is an effective method, and postoperative prognosis is good. There may be multiple lesions, so long-term follow-up is needed.

          Release date:2016-08-31 05:44 Export PDF Favorites Scan
        • Clinical Study of Conservative Treatment for 120 Patients with Granulomatous Mastitis

          ObjectiveTo investigate etiology of granulomatous mastitis and it,s conservative treatment method. MethodThe clinical data of 120 patients with granulomatous mastitis given drugs for closed treatment plus massage dredge and ductal lavage from January 2011 to December 2012 in this hospital were analyzed retrospectively. ResultsOne hundred and one cases were cured following conservative treatment for 2 to 8 weeks,19 cases were underwent surgical treatment because of poor outcome.Nine of 101(8.9%) cured patients were relapsed for following-up of 30 to 42 months. ConclusionClosed treatment with drugs,which is effective,could keep patient with granulomatous mastitis from having mastectomy and reduce recurrence.

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