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小儿支气管迪厄拉富瓦病伴膈下动脉供血反复咯血1例报告

Recurrent hemoptysis in pediatric bronchial Dieulafoy's disease with inferior phrenic artery supply: A case report.

作者信息

Wang Fang, Tang Jiao, Peng Mou, Huang Pu-Jue, Zhao Li-Juan, Zhang Yin-Yue, Wang Tao

机构信息

Department of Pediatric Cardiology, West China Second University Hospital, Sichuan University, Chengdu 610041, Sichuan Province, China.

Department of Pediatrics, The First People's Hospital of Longquanyi District, Chengdu 610041, Sichuan Province, China.

出版信息

World J Clin Cases. 2023 Sep 16;11(26):6268-6273. doi: 10.12998/wjcc.v11.i26.6268.

Abstract

BACKGROUND

Bronchial Dieulafoy's disease (BDD) is characterized by the erosion of an anomalous artery in the submucosa of the bronchus. The etiology of pediatric BDD is mainly congenital dysplasia of bronchus and pulmonary arteries, which is different from chronic inflammatory injury of the airway in adult patients. The internal thoracic artery, subclavian artery, and intercostal artery are known to be involved in the blood supply to the BDD lesion in children.

CASE SUMMARY

We report a case of BDD in a 4-year-old boy with recurrent hemoptysis for one year. Selective angiography showed a dilated right bronchial artery, and anastomosis of its branches with the right lower pulmonary vascular network. Bronchoscopy showed nodular protrusion of the bronchial mucosa with a local scar. Selective embolization of the bronchial artery was performed to stop bleeding. One month after the first intervention, the symptoms of hemoptysis recurred. A computed tomography angiogram (CTA) showed another tortuous and dilated feeding artery in the right lower lung, which was an abnormal ascending branch of the inferior phrenic artery (IPA). The results of angiography were consistent with the CTA findings. The IPA was found to be another main supplying artery, which was not considered during the first intervention. Finally, the IPA was also treated by microsphere embolization combined with coil interventional closure. During the one-year follow-up, the patient never experienced hemoptysis.

CONCLUSION

The supplying arteries of the bleeding lesion in children with BDD may originate from multiple different aortopulmonary collateral arteries, and the IPA should be considered to reduce missed diagnosis. CTA is a noninvasive radiological examination for the screening of suspected vessels, which shows a high coincidence with angiography, and can serve as the first choice for the diagnosis of BDD.

摘要

背景

支气管迪厄拉富瓦病(BDD)的特征是支气管黏膜下层的异常动脉发生糜烂。小儿BDD的病因主要是支气管和肺动脉的先天性发育异常,这与成年患者气道的慢性炎症损伤不同。已知胸廓内动脉、锁骨下动脉和肋间动脉参与小儿BDD病变的血液供应。

病例摘要

我们报告一例4岁男孩BDD,反复咯血1年。选择性血管造影显示右支气管动脉扩张,其分支与右下肺血管网吻合。支气管镜检查显示支气管黏膜结节状突出并伴有局部瘢痕。对支气管动脉进行选择性栓塞以止血。首次干预1个月后,咯血症状复发。计算机断层血管造影(CTA)显示右下肺另有一条迂曲扩张的供血动脉,是膈下动脉(IPA)的异常升支。血管造影结果与CTA检查结果一致。发现IPA是另一条主要供血动脉,首次干预时未考虑到。最后,对IPA也采用微球栓塞联合弹簧圈介入封堵治疗。在1年的随访中,患者未再咯血。

结论

小儿BDD出血病变的供血动脉可能源自多条不同的主-肺动脉侧支动脉,应考虑到IPA以减少漏诊。CTA是一种用于筛查可疑血管的无创性影像学检查,与血管造影显示出高度一致性,可作为BDD诊断的首选方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b5e/10507539/ec36267622ee/WJCC-11-6268-g001.jpg

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