Zhang Ruifeng, Ma Guofeng, Xu Xiaoling, Liang Li
Department of Respiratory Medicine, Sir Run Run Shaw Hospital, Medical School of Zhejiang University, Hangzhou, Zhejiang, China.
Medicine (Baltimore). 2018 Jan;97(2):e9469. doi: 10.1097/MD.0000000000009469.
Exposure to crystalline silica results in silicosis with initiation and progression of pulmonary fibrosis. The impaired lung parenchyma leads to pulmonary arterial hypertension and increased pressure in the right ventricle of the heart. Usually, the silicosis may be followed by enlargement of hilar lymphnodes, but silicosis-induced pulmonary artery stenosis with severe pulmonary hypertension is rare. Percutaneous pulmonary artery stenting and balloon angioplasty were performed to relieve stenosis and pulmonary hypertension.
We report the case of a 52-year-old man who was admitted for persistent dyspnea for 2 years and progressive dyspnea for half a month. He had been a stonemason for 20 years. The computer tomography pulmonary angiography scan images showed partially fibrotic lungs with a disseminated nodular pattern and enlarged bilateral hilar and mediastinal lymphnodes. The echocardiogram and right heart catheterization confirmed the diagnosis of severe pulmonary arterial hypertension.
Pulmonary angiograms showed severe stenosis of the proximal upper right and lower left pulmonary artery. Moderate stenosis occured in a branch of the lower right pulmonary artery and a branch of the upper left pulmonary artery. A total of 2 stents and 4 balloons were used to relieve lesions. The final angiograms showed a significantly increased pulmonary artery caliber. The clinical symptom and 6-minute walk distance of the patient were much improved.
To our knowledge, this is the first reported case of percutaneous treatment for silicosis-induced pulmonary artery stenosis and pulmonary hypertension. The clinical symptom, 6-minute walking test, and vessel caliber at areas of stenosis improved significantly following stent implantation and balloon dilatation. However, the patient was followed up for a short period and long-term outcomes have not yet been sufficiently evaluated.
接触结晶二氧化硅会导致矽肺,并引发和加剧肺纤维化。肺实质受损会导致肺动脉高压以及右心室压力升高。通常,矽肺之后可能会出现肺门淋巴结肿大,但由矽肺引起的伴有严重肺动脉高压的肺动脉狭窄却很罕见。已实施经皮肺动脉支架置入术和球囊血管成形术来缓解狭窄和肺动脉高压。
我们报告了一名52岁男性的病例,他因持续两年的呼吸困难以及近半个月来逐渐加重的呼吸困难入院。他曾做过20年石匠。计算机断层扫描肺动脉造影扫描图像显示肺部部分纤维化,呈弥漫性结节状,双侧肺门和纵隔淋巴结肿大。超声心动图和右心导管检查确诊为严重肺动脉高压。
肺动脉造影显示右上肺动脉近端和左下肺动脉严重狭窄。右下肺动脉一个分支和左上肺动脉一个分支出现中度狭窄。共使用了2个支架和4个球囊来缓解病变。最终造影显示肺动脉管径明显增大。患者的临床症状和6分钟步行距离有了显著改善。
据我们所知,这是首例关于经皮治疗矽肺所致肺动脉狭窄和肺动脉高压的报道病例。支架植入和球囊扩张后,临床症状、6分钟步行试验以及狭窄部位的血管管径均有显著改善。然而,该患者随访时间较短,长期疗效尚未得到充分评估。