Objective To explore the X-ray diagnosis of diffuse pulmonary disease.

Complications include heart failure, pulmonary edema , and high potassium levels.

并发症包括心力衰竭 、 肺水肿及血钾过多.

Pulmonary edema is a condition caused by excess fluid in the lungs.

肺水肿是过多液体积聚在肺内导致的疾病.

Bloody foam around the mouth indicates pulmonary edema.

嘴巴周围的血表明了他有肺水肿.

It is a rare, but rather benign pulmonary edema.

它虽然罕见, 却是个预后不错的疾病.

Phosgene poisoning can cause pulmonary edema and even ARDS.

光气中毒可引起迟发性肺水肿甚至急性呼吸窘迫综合征(ARDS).

Excessive acute exposure may cause delayed pulmonary edema ( fluid buildup ) to occur.

过分剧烈暴露会导致肺水肿 ( 流体积累 ).

The lungs should be examined for possible pulmonary edema.

应检查肺部,视其是否有肺水肿.

Objective : To investigate about observation point and nursing measure of reexpansin pulmonary edema.

目的: 探讨复张性肺水肿的观察要点与治疗措施.

Measurement: Prospectiely diagnosed and confirmed symptomatic deep venous thrombosis or pulmonary embolism.

测量指标――预期诊断和被证实为有症状的深部静脉血栓形成或者肺栓塞.

Angiography in the Diagnosis of Acute Massive Pulmonary Embolism.

血管造影诊断急性大块肺栓塞.

ConclusionColor Doppler sonography is the first choice in the diagnosis and differential diagnosis of pulmonary embolism.

结论彩色多普勒超声是肺动脉栓塞影像学诊断和鉴别诊断的首选手段.

Idiopathic pulmonary fibrosis ( IPF ) has a poor prognosis and a course that is unpredictable.

特 发性 肺纤维化预后不佳,其发展过程无法预知.

Abstract: Objective To observe ultrastructural changes and study the pathogenesis of idiopathic pulmonary fibrosis.

文摘: 目的观察特发性肺纤维化的超微结构变化并探讨其发病机理.

Only about 1 % of such persons get a significant degree of pulmonary fibrosis.

仅有大约1%的这种病人出现明显的肺纤维化.

Objective To observe ultrastructural changes and study the pathogenesis of idiopathic pulmonary fibrosis.

目的观察特发性肺纤维化的超微结构变化并探讨其发病机理.

Pulmonary fibrosis is an important toxic effect of paraquat.

在各种肺组织损伤中又以肺纤维化损伤最为突出.

Background Bloemycin ( BLM ) induced pulmonary fibrosis ( BPF ) is most widely used animal model for idiopathic pulmonary fibrosis.

博莱霉素 ( BLM ) 所致的肺纤维化 ( BPF ) 模型是最常用的研究特发性肺纤维化的动物模型.

At the provincial hospital diagnosis of systemic sclerosis with pulmonary fibrosis.

在省医院住院诊断为系统性硬化症合并肺间质纤维化.

Objective : To explore the effect and molecular mechanism of Qidankeli in the treatment of pulmonary fibrosis.

目的探讨芪丹颗粒治疗肺间质纤维化的效果及分子作用机制.

Idiopathic pulmonary fibrosis: acting or waiting?

特发性肺纤维化: 治疗还是等待?