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find Author "王发平" 4 results
  • Clinical characteristics of bone marrow tuberculosis and literature review

    Objective To improve the knowledge of bone marrow tuberculosis by summarizing the risk factors, clinical features, diagnosis, therapeutic response and prognosis. Methods The medical records of 62 patients with bone marrow tuberculosis from January 2004 to December 2014 were retrospectively analyzed. Results The patients included 34 males and 28 females. Their age ranged from 15 to 80 years with a mean age of 45.3±35.7 years. Among them, 21 cases (33.9%) had one or more risk factors such as advanced kidney disease or liver disease, chronic respiratory disease, rheumatoid immune system disease and diabetes. No specific clinical features were found in patients with bone marrow tuberculosis, and the most common symptom was fever (98.4%). Blood routine examination revealed that variety of hematological abnormalities include leucopenia, thrombocytopenia, anemia or pancytopenia occurred in 59 patients (95.2%). Chest CT scan showed typical disseminated tuberculosis in 22 patients (36.1%), secondary pulmonary tuberculosis in 6 patients (9.8%), and atypical manifestations of tuberculosis in 26 patients (42.6%). The common patterns of abdomen abnormalities on ultrasonic testing or CT scan were hepatosplenomegaly. Bone marrow biopsy was performed in all the 62 patients, among them, the needle-aspirated bone marrow specimens showed granulomatous lesions in 53 patients (85.5%). The acid-fast staining of bone marrow smear was performed in a total of 57 patients, which was positive in 28 patients (49.1%). Twenty-five patients completed phone call follow-up, and 8 patients died from bone marrow tuberculosis and its complications. Conclusions Bone marrow tuberculosis is a rare manifestation of disseminated tuberculosis. The common symptom of this disease is pyrexia . The clinical presentations and laboratory examinations of this disease are nonspecific. Bone marrow biopsy is a major method for diagnosis. Part of patients with bone marrow tuberculosis lack of imaging proof for lung lesion. Therefore, we should heighten vigilance for bone marrow tuberculosis in patients with fever of unknown origin.

    Release date:2017-04-01 08:56 Export PDF Favorites Scan
  • Airway hemangioma: a case report and literature review

    ObjectiveTo explore the clinical features, diagnosis, differential diagnosis, pathological characteristics, management and prognosis of airway hemangioma, and improve the level of the diagnosis and therapy.MethodsThe clinical data of a patient with airway hemangioma admitted to West China Hospital of Sichuan University were retrospectively analyzed. The related literatures were reviewed. Databases including PubMed, Ovid Medline, Embase, VIP, Wanfang and Chinese National Knowledge infrastructure were searched using the keywords as " Trachea” OR " Bronchus” AND " Hemangioma” from January 1976 to October 2016.ResultsThe patient was a 32-year-old male presented with hemoptysis and backache more than 10 days. His enhanced chest CT scan revealed thickening of the esophagus wall and narrowing of the lumen of esophagus. A wide range of vascular tumor like changes in the trachea and the two sides of bronchus were found by the fiberoptic bronchoscopy and gastroscope examination suggested esophageal varices. Although the patient had a wide range of airway lesions, the symptom of hemoptysis was relieved after the conservative treatment. The patient’s condition was stable until now. From January 1976 to October 2016, a total of 34 related articles were retrieved and 36 cases of airway hemangioma were reported. The etiology of the disease remains unknown. Recurrent hemoptysis was the common symptoms of airway hemangioma, and imaging changes lacking characteristics. Histopathological examination revealed dilated, thin-walled and different size of vascular or hyperplastic capillary and immunohistochemical staining was positive for vascular endothelial cell specific CD34 and Ⅷ factor.ConclusionsHemangioma is a common benign tumor of head and neck in infants and children. Hemangioma is very rarely occurred in trachea in adults. Clinical and imaging manifestations are not specific, and diagnosis relies on histopathological examination. Fiberoptic bronchoscopy and three dimensional reconstruction of thoracic vessels with CT play important roles in the whole process of diagnosis and treatment of airway hemangioma. It should be differentiated from lymphangioma. The prognosis of airway hemangioma is good.

    Release date:2017-07-24 01:54 Export PDF Favorites Scan
  • 胸膜上皮样血管内皮细胞瘤一例并文献复习

    目的探讨胸膜上皮样血管内皮细胞瘤(PEH)的临床表现、影像、病理学特征、诊断、鉴别诊断、治疗及预后, 提高对该病的诊治水平。 方法以"胸膜上皮样血管内皮细胞瘤"为检索词检索了四川大学华西医院2007年1月至2014年12月的住院患者资料, 仅有1例呼吸内科收治的患者符合条件, 就此回顾性分析其临床特点, 并进行相关文献复习。以"胸膜上皮样血管内皮细胞瘤"为检索词检索万方数据库和中国期刊网全文数据库, 以"pleural epithelioid hemangioendothelioma"为检索词检索PubMed、Embase、Ovid及Cochrane数据库, 检索时间为1975年1月至2015年4月。 结果68岁女性患者, 临床表现胸背痛, 查体发现除左侧胸腔积液体征外, 有新近发生的脊柱侧弯畸形及杵状指。胸部增强CT示左侧胸膜弥漫增厚伴胸腔大量积液, 部分包裹, 左肺舌叶及下叶压迫性不张, 不张舌叶内见密度减低影, 右肺散在结节。经胸膜活检获得病理, 组织学上查见异型细胞巢, 进一步免疫组化染色血小板内皮细胞黏附分子(CD31)蛋白阳性, 至此明确诊断。本例患者拒绝化疗, 明确诊断11个月后死亡。文献复习显示, 在上述数据库中共检索到74篇文献, 经筛选后, 有26篇文献40例患者明确诊断为PEH且具备相应临床资料, 符合检索条件。此类患者主要的临床表现为胸痛及呼吸困难, 影像学主要表现为胸腔积液, 胸膜不规则增厚, 组织病理学呈现血管内皮源性免疫标志物阳性。 结论PEH为罕见的低度恶性血管源性肿瘤, 病因不清, 临床表现及影像学不具有特征性, 与肿瘤胸膜转移、胸膜间皮瘤等疾病易混淆, 其诊断主要依靠活检组织病理学检查。现有的治疗手段有限, 尚无有效的治疗措施。预后与性别、年龄及病变累计范围等多种因素有关。

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  • 茚达特罗在慢性阻塞性肺疾病中的临床应用

    Release date:2019-05-23 04:40 Export PDF Favorites Scan
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