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find Keyword "肉芽肿" 41 results
  • 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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  • 变应性肉芽肿性血管炎两例并文献复习

    变应性肉芽肿性血管炎又称Churg—Strauss综合征(CSS ),是一种以哮喘、血和组织中嗜酸粒细胞增多、血管外坏死性肉芽肿为特征的系统性小血管炎。该病临床罕见,国外报道其发病率约为24/100万。由于该病早期临床表现不典型,容易误诊,现将我院收治的2例CSS患者报告如下。临床资料 例1 患者男性,56岁。因“反复胸闷气喘伴咳嗽28个月,双手发麻6个月,加重10 d”,于2007年12月1日入院。2005年8月起无明显诱因经常感胸闷气喘,活动时明显,伴咳嗽,咳少量白色黏痰,在外院诊断为肺炎,经抗感染治疗可好转。2006年6月2日胸部CT示两肺纹理粗乱,右中叶、左舌叶见少许小片状影;2006年6月6日支气管镜检查见气管支气管黏膜充血水肿,腔内少量白色分泌物;痰找抗酸杆菌阳性,于2006年6月7日第1次住院。病程中,体重减轻10 kg。既往于2005年5月22日因双侧锁骨上窝淋巴结肿大行淋巴结活检,活检病理示慢性反应性增生;1:2000 PPD试验 红肿大小为10 mm×11 mm,有水泡。查体:双肺未闻及干湿性啰音。入院后查血常规:白细胞(WBC)总数11.1×109/L,血红蛋白96 g/L,血小板计数192×109/L;血结核抗体弱阳性(酶标法);肝功能:球蛋白82.1 g/L,白蛋白28.3 g/L;肾功能正常;血沉 115 mm/1 h;尿常规:潜血(±),痰找结核菌6次阴性;腹部CT平扫+增强提示右肾上腺肿瘤(嗜铬细胞瘤可能性大);心脏彩超及动脉血气正常。诊断为肺结核,支气管结核,右肾上腺嗜铬细胞瘤,于2006年6月19日予3HLEZ/9HL方案抗结核及抗感染治疗,2006年6月26日症状好转出院,但仍感活动时胸闷气喘,复查血常规:WBC总数8.3×109/L,血红蛋白95 g/L,血小板计数400×109/L;肝功能:球蛋白68.5 g/L,白蛋白26.3 g/L;肾功能正常。于2006年9月1日因双下肢关节痛自行停用抗结核治疗。2006年9月11日行右肾上腺嗜铬细胞瘤切除治疗。

    Release date:2016-08-30 11:58 Export PDF Favorites Scan
  • Progress in diagnosis and treatment of granulomatous lobular mastitis

    ObjectiveTo investigate the research progress of etiology, pathogenesis, diagnosis, differential diagnosis, and treatment of granulomatous lobular mastitis (GLM). MethodA comprehensive analysis was conducted by reviewing the domestic and foreign literatures on GLM and combining with clinical experience. ResultsGLM was a relatively rare chronic inflammatory disease of the breast, and the number of patients had been increasing in recent years. It mainly occured in multiparous women of childbearing age. Clinically, it was characterized by a hard breast mass with or without redness and pain, and severe cases might be accompanied by nodular erythema and arthritis. Bacterial infection, especially Corynebacterium kroppenstedtii and autoimmunity were considered to be the main causes of GLM. The diagnosis of GLM needed to combine with medical history, clinical manifestations, histopathological findings, imaging findings, and laboratory tests. A multidisciplinary team for diagnosis and treatment of GLM should be established to improve the diagnostic accuracy and reduce misdiagnosis. At present, the treatment methods for GLM were mainly conservative treatment and surgical treatment, including follow-up observation, antibiotic treatment, glucocorticoid treatment, immunosuppressive therapy, surgical treatment, traditional Chinese medicine treatment, and combined treatment. ConclusionsAt present, the incidence of GLM is on the rise, but its etiology and pathogenesis are still unclear. The diagnosis needs to combine with many aspects, and it is recommended that the multidisciplinary team could improve the accuracy of diagnosis. There is still no unified standard for the selection and timing of treatment. Clinicians’ experience and patients’ wishes should be taken into account when choosing treatment options in clinical practice. Prospective and high-quality multicenter clinical trials and evidence-based medicine practice are still needed to further improve diagnosis and treatment of GLM.

    Release date:2023-12-26 06:00 Export PDF Favorites Scan
  • 坏死性肉芽肿性血管炎一例误诊分析并文献复习

    坏死性肉芽肿性血管炎( necrotizing granulomatous vasculitis, NGV) 是一种病因未明的系统性血管炎[ 1] , 临床上分全身型和局限型[ 2 ] 。全身型以上、下呼吸道和肾脏为常见受累器官, 无肾脏受累者则为局限型。该病男性略多于女性, 40 ~50 岁为高发年龄段。因其临床表现多样, 且无特异性, 常误诊为各亚专科疾病[ 3 ] 。2012 年11 月6 日, 郑州大学第一附属医院呼吸及睡眠科收治1 例青年女性NGV患者, 现结合文献复习如下。

    Release date:2016-09-13 03:54 Export PDF Favorites Scan
  • 变应性肉芽肿性血管炎二例报告并文献复习

    目的 加深对变应性肉芽肿性血管炎(又称Churg-Strauss综合征,CSS)的认识,提高临床诊断及治疗水平,改善预后。方法 复习国内发表的临床诊断为CSS的28例病例,结合近期南华大学第二附属医院收治的2例变应性肉芽肿性血管炎病例进行临床分析。结果 30例患者中,男16例(53.3%),女14例(46.7%);年龄7~76岁,平均41.4岁。14例以喘息为首发症状,19例有支气管哮喘症状,病变可累及呼吸系统(63.3%)、神经系统(36.7%)、皮肤(50.0%)、消化系统(33.3%)、心脏(13.3%)、肾脏(6.7%)、关节肌肉(3.0%)、外周血管(6.7%)及眼部(6.7%)等。28例(93.3%)存在嗜酸粒细胞异常,平均值为29.5%,6例患者抗中性粒细胞胞浆抗体核周型(P-ANCA)、抗中性粒细胞胞浆抗体胞浆型(C-ANCA)检查均提示阳性。18例CSS患者肺部CT存在异常,多表现为浸润性、磨玻璃样、弥漫性间质样或结节样改变;14例取得病理学检查依据,表现为嗜酸粒细胞浸润,血管炎及血管外肉芽肿。临床治疗主要使用糖皮质激素和免疫抑制剂(如环磷酰胺),总体预后较好。结论 变应性肉芽肿性血管炎是一种罕见的系统性血管炎疾病,临床表现缺乏特异性,易漏诊、误诊,当患者表现为哮喘、外周血嗜酸粒细胞增多及肉芽肿性血管炎时,应高度警惕此病。

    Release date:2016-08-30 11:31 Export PDF Favorites Scan
  • 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
  • Analysis of Diagnosis and Treatment of Xanthogranulomatous Cholecystitis in 48 Cases

    ObjectiveTo explore the etiological agent, clinical manifestations, imaging findings, pathologic characteristics, diagnosis, treatment, and prognosis of xanthogranulomatous cholecystitis(XGC). MethodThe clinical data of 48 patients with XGC diagnosed by postoperative pathology from January 2003 to December 2012 were collected and analyzed. ResultsIn these 48 patients with XGC, the clinical manifestations included 40(83.3%)patients with upper right abdominal pain, 18(37.5%)patients with jaundice, 12(25.0%)patients with fever. B ultrasound examination was performed in 45 cases, in which 42 cases were diagnosed with cholecystitis, 38 cases together with cholecystolithiasis, 15 cases together with cholecystolithiasis and gallbladder neoplasm, and 3 cases together with choledocholith with bile duct dilatation. CT was performed in 30 cases, in which 25 cases were diagnosed with cholecystitis together with cholecystolithiasis, 11 cases were diagnosed with gallbladder neoplasm. MRI was performed in 22 cases, in which 18 cases were diagnosed with cholecystitis together with cholecystolithiasis, 4 cases were diagnosed with gallbladder carcinoma. Thirty-three cases were treated with open cholecystectomy, 9 patients with laparoscopic cholecystectomy, 4 patients with cholecystectomy plus choledocholithotomy and T-tube drainage, 2 patients with cholecystectomy plus partial hepatectomy. All the patients were diagnosed with XGC by postoperative pathology and recovered well without recurrence and canceration. ConclusionsXGC is a kind of benign and invasive disease without specific clinical manifestation. Bultrasound, CT, or MRI play an important role in diagnosis, but final diagnosis is mainly based on pathological detection, and surgery is the most effective treatment. The prognosis of XGC is favorable if gallbladder is completely resected.

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  • 伴发癫痫的侧脑室脉络丛黄色肉芽肿一例

    Release date:2023-09-07 11:00 Export PDF Favorites Scan
  • Clinical Analysis of Granulomatous Lung Disease: 36 Cases Report

    Objective To analyze the data from patients with pathologically proved granulomatous lung disease, including etiology, clinical, radiological features and laboratory results. Methods 36 patients with granulomatous lung disease confirmed by lung biopsy in Shanghai First People’s Hospital of Shanghai Jiao Tong University from January 2008 to June 2012 were retrospectively reviewed. The clinical presentation, radiological features and laboratory results were collected and statistically analyzed.Results After haematoxylin and eosin stain combined with special stain, the diagnoses were comfirmed, ie.13 cases of mycobacterial infection, 5 cases of aspergillar infection, 4 cases of cryptococcal infection, 6 cases of sarcoidosis, 4 cases of Wegener’s granulomatosis, 4 cases of unknown causes. Cough was the most common clinical symptom, followed by expectoration. Some patients also developed fever, chest tightness and weight loss. The lesions were widely distributed, of which the right upper lung was the common lesion of mycobacterial infection, inferior lobe of right lung was the common lesion of aspergillar infection. The common lesion of cryptococcal infection was uncertain. The common lesions of sarcoidosis and Wegener ’s granulomatosis were in left upper lung. Small nodule was the most common shapes of lesion, while mass and consolidation were present sometimes. Cavity, air bronchogram, pleural effusion, hilar and mediastinal lymph node enlargement could be found in the chest CT. Interferon gamma release assay, galactomannan antigen assay and latex agglutination test were helpful in the diagnosis of mycobacterial infection, aspergillar infection and cryptococcal infection induced granuloma. Conclusions The clinical presentations and radiological features of granulomatous lung disease are nonspecific. Histopathology obtained through biopsy is the key for the diagnosis. Immunological examination, test of new antigens to microorganism and clinical microorganism detection are valuble in the diagnosis and differential diagnosis of granulomatous lung disease.

    Release date:2016-09-13 03:51 Export PDF Favorites Scan
  • 肉芽肿性多血管炎致中枢性尿崩症一例并文献复习

    目的探讨肉芽肿性多血管炎累及垂体的临床表现、影像学特点、治疗及预后。方法对 1 例确诊的肉芽肿性多血管炎致中枢性尿崩症患者的临床资料结合文献复习进行分析,总结其临床特点、治疗及预后。结果本例患者为女性,66 岁,以耳、鼻受损为首发症状,合并肺部、肾脏病变,垂体受累表现为中枢性尿崩症及垂体后叶高信号消失,糖皮质激素诱导治疗后尿崩症缓解。结合文献复习,肉芽肿性多血管炎是最常出现垂体病变的血管炎类型,发病率 1% 左右,好发于女性,多数表现为中枢性尿崩症,其次是腺垂体功能减退、高泌乳素血症。典型的垂体磁共振成像病变征象为 T1 加权相上垂体后叶高信号消失。既往多采用糖皮质激素联合环磷酰胺的诱导缓解方案,但因治疗不及时多数患者不能恢复正常垂体功能。结论肉芽肿性多血管炎累及垂体的情况极为罕见且起病隐匿。尿崩症通常为首发症状或与耳鼻喉症状伴行,肺、肾脏受累症状轻、出现迟。早期诊断和及时治疗有利于减少垂体的不可逆损伤,保存正常垂体功能。

    Release date:2020-01-15 11:30 Export PDF Favorites Scan
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