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lymphadenopathy相关的网络例句

查询词典 lymphadenopathy

与 lymphadenopathy 相关的网络例句 [注:此内容来源于网络,仅供参考]

Results The lesion located at the basal segments of left lower lobe in 9 cases (90%), furthermore, 7(70%) at the posterior basal segments; The remainder 1 case (10%) was found at the posterior basal segment of right lower lobe; The lesion present as multiloculated cyst containing fluid and/or air in 7 cases(70%) without contrast enhancement of cyst wall, 3 cases (30%) presented as irregular mass with moderate enhancement, in which bronchiectasis with mucous impaction, calcification or cyst containing fluid may be seen; MRP, MIP and VR reconstructions showed anomalous branches arising from descending aorta in all 10 patients(100%) with draining into left atrium via pulmonary vein,which was consistent with surgery; Ipsilateral hilar lymphadenopathy was demonstrated in 7 cases (70%).

结果 9例(90%)病灶位于左下叶基底段,其中7例(70%)位于左下叶后基底段,1例(10%)位于右下叶后基底段;7例(70%)病灶表现为含液/气的薄壁多房囊腔,增强后囊壁无明显强化,3例(30%)表现为不规则团块,增强后有中等强化,其内有粘液嵌塞的扩张支气管,也可有钙化或液性区;MPR、MIP及VR等三维重建显示10例(100%)均为降主动脉发出异常分支供血,并通过肺静脉回流入左房,血管显示情况与手术相符;7例(70%)患侧肺门淋巴结有增大。

Diarrhea, anemia, lymphadenopathy and skin lesions, especially necrotic papular eruptions.

结果本组患者以反复发热、咳嗽、消瘦、腹泻、贫血、淋巴结肿大。

These clinical data suggest that any manifestations similiar to pulmonary interstitial fibrosis complicated with pleural effusion and paratracheal lymphadenopathy should be further differentiated from PLC by HRCT and pleural-lung tissue biopsy.

对双肺呈类间质纤维化改变,同时合并胸腔积液和纵隔淋巴结肿大的患者,应进一步行高分辨CT及胸膜肺组织病理活检,以期排除PLC之诊断。

The morphologic features including tumor size, contrast enhanced pattern,invasion of perinephric fat, renal vein and inferior vena cava as well as lymphadenopathy were evaluated.

搜集2002年以来26例行CT检查并经病理证实为肾癌患者的病例资料,在CT平扫及三期动态增强扫描图像上对肿瘤的大小、强化模式、肾周改变、邻近脏器及静脉的受侵情况和淋巴结转移等征象进行分析和评价。

Results Among 94 cases, 79 cases who were preoperatively diagnosed with unknown mediastinal mass or lymphadenopathy by chest Computer tomography did not obtain the pathological cell by bronchoscopy, sputum cytology or percutaneous pneumocentesis biopsy, by SCM, 74 cases obtained the pathological diagnosis, while the other 5 cases did not obtain the pathological diagnosis.

结果 其中79例CT显示不明原因的纵隔肿物或纵隔淋巴结肿大,且纤维支气管镜和痰脱落细胞学或经皮肺穿刺未找到病理细胞,纵隔镜检查后74例获得病理诊断,5例未获病理明确。

We describe a 13 year old boy who complained of soft, postauricular, non-tender, progressively enlarging masses bilaterally that had been present for a number of years with associated bilateral neck lymphadenopathy.

此病例为13岁男性,主述双侧耳后肿块渐渐变大有数年的时间,摸起来柔软,并无疼痛及压痛感,合并有双侧颈部淋巴结肿大。

In addition, shotty anterior cervical lymphadenopathy was noted.

此外,记录了颈前淋巴结小弹丸样病变。

Most patients had a history of working in open field, and presented as high fever, skin eschars, ulcers or rashes and lymphadenopathy.

结果 符合诊断标准的男43例,女57例,年龄1.5~80岁(平均30岁),6~9月为发病高峰,多有野外作业史。

For 21 cases of thyroid malignant nodule, 17 showed untidy margin and clear borderlines were detected in 4 cases; 8 cases had vesica and 9 had calcification; 6 cases showed no complete enhanced ring around the tumor, and 7 cases were revealed metastatic lymphadenopathy on the neck.

结果 47例单发良性结节中39例病变边界清晰、8例病灶边界欠清、26例囊变、10例钙化;21例恶性结节有17例病变边界不清、4例病灶边界较清、8例囊变、9例钙化、6例表现强化残圈征、9例肿瘤侵犯周围组织器官和7例颈部淋巴结转移。

Patients developed head cervical lymph node swelling. The lymph node biopsy revealed a background of reactive lymphadenopathy and necrosis in some cases and apoptosis, nuclear debris in all cases, loss of lymph node structure, proliferation of lymphocytes and various types histiocytes with phagocytosis, no infiltration of neutrophils. Three histological types: proliferative, necrotizing and xanthomatous were classified.

形态特征为在活跃的反应性增生淋巴结病变的背景下,出现不同程度的凝固性坏死,淋巴细胞凋亡及核碎片几乎见于所有病例,伴有多种形态的组织细胞增生,吞噬现象明显,无中性杜白细胞浸润,组织学上可分为3型:增生型,坏死型及黄色瘤样型。

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