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- primary pulmonary hypertensoin 原发性肺动脉高(血)压
- Primary pulmonary artery sarcoma is a rare tumor. 摘要肺动脉肉瘤是一种罕见的肿瘤。
- Objective:To investigate the clinical and CT findings of primary pulmonary cryptococcosis ( PPC). 目的:探讨原发性肺隐球菌病的临床与CT诊断。
- Objective: To study the prognosis of surgical treatment of primary pulmonary malignant fibrous histocytoma (MFH). 摘要目的:研究经外科手术治疗的肺原发恶性纤维组织细胞瘤的临床特点及其预后。
- Primary pulmonary ACA, also known as the Fechner tumor, is rare with only 11 cases described in the literature. 在所报道的文献中,很少见有涎腺原发的腺泡细胞腺癌出现肺转移。
- Objective: To introduce inhaled iloprost for the treatment of primary pulmonary hypertension. 摘要目的:介绍治疗原发性肺动脉高压的吸入性伊洛前列素。
- PPL accounted for 10 (0.5%) of 1887 cases of primary pulmonary malignant carcinoma in the same period, and PLG for 2 (0.1%) of 1887 cases. PPL和PLG分别占同期手术的肺恶性肿瘤的0.;5%25(10/1887)和0
- Results and Conclusion: Inhaled iloprost can reduce pulmonary vascular resistance and delay the development of primary pulmonary hypertension. 结果和结伦:吸入性伊洛前列素治疗可以降低肺血管阻力和延缓原发性肺动脉高压的进程。
- Objective To investigate the clinical and pathological characteristics of primary pulmonary plasmacytoma (PPP) and its diagnosis and treatment. 目的了解原发性肺浆细胞瘤的临床表现、病理表现及诊治。
- Result primary pulmonary lymphoma was easy to be misdiagnosed to other pulmonary disease due to lack of specific characteristics. 结果原发于肺的淋巴瘤无特异性临床表现和影像改变,易误诊。
- Results Primary pulmonary choriocarcinoma in men , which contained syncytiotrophoblastic cells, was one of the highly malignant tumors. 结果男性肺原发性绒毛膜癌是一种恶性程度很高的肿瘤,包含合体滋养层细胞。
- Results and Conclusion:Inhaled iloprost can reduce pulmonary vascular resistance and delay the development of primary pulmonary hypertension. 结果和结论:吸入性伊洛前列素治疗可以降低肺血管阻力和延缓原发性肺动脉高压的进程。
- Methods One male patient with primary pulmonary choriocarcinoma confirmed by exploratory thoracotomy and biopsy, and relevant literatures were reviewed. 方法对1例经开胸肺活检确诊为男性肺原发性绒毛膜癌患者的临床资料进行分析,并结合文献进行复习。
- Methods: The clinical data of 6 patients with primary pulmonary hypertension were collected and analyzed.Clinical diagnosis was made by ways of electrocardiography, ultrasound, and X-ray. 方法:对6例确诊为原发性肺动脉高压患儿从临床症状和体征、辅助检查、心导管和心血管造影术等方面进行分析。
- primary pulmonary arterial dilatation 原发性肺动脉扩张
- primary pulmonary hypertension syndrome 原发性肺动脉高压综合征
- North American primary pulmonary blastomycosis 北美原发性肺芽生菌病
- Primary pulmonary coccidioidomycosis 原发性肺球孢子菌病
- primary pulmonary histoplasmosis 原发性肺组织胞浆菌病
- familial primary pulmonary hypertension 家族性原发性肺动脉高压