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先天性心脏异常中的肺部超声:永存动脉干。

Lung Ultrasound in Congenital Cardiac Abnormality: ALCAPA.

机构信息

Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli, IRCCS, Rome, Italy.

Università Cattolica del Sacro Cuore, Rome, Italy.

出版信息

Indian J Pediatr. 2021 Feb;88(2):161-164. doi: 10.1007/s12098-020-03208-z. Epub 2020 Feb 11.

Abstract

Anomalous origin of left coronary artery from the pulmonary artery (ALCAPA) is a life-threatening ischemic congenital cardiac disease, resulting in myocardial dysfunction and heart failure within the first year of life. The authors report the case of a 1-mo-old infant with a radiological diagnosis of pneumonia handled with point-of-care lung ultrasound (POCUS) due to the persistence of dyspnea, despite a week of antibiotic therapy. Lung ultrasound showed a non-univocal interpretation of the lesion and gave indication to the second level instrumental diagnostics that confirmed the presence of ALCAPA. There is no case of lung ultrasound aiding to the early diagnosis of ALCAPA and no indirect ecographic signs of ALCAPA that have been described in literature yet.

摘要

左冠状动脉起源于肺动脉(ALCAPA)异常是一种危及生命的缺血性先天性心脏病,可导致生命的第一年心肌功能障碍和心力衰竭。作者报告了一例 1 个月大的婴儿,因呼吸困难持续存在,尽管已接受一周的抗生素治疗,但仍经床边肺部超声(POCUS)进行放射学诊断为肺炎。肺部超声显示病变的解释不明确,并提示进行二级仪器诊断,以确认存在 ALCAPA。目前尚无肺部超声有助于早期诊断 ALCAPA 的病例,也没有文献中描述的 ALCAPA 的间接超声征象。

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