一名新生儿先天性肺气道畸形，表现为严重呼吸窘迫和气胸。
Congenital pulmonary airway malformation manifesting with severe respiratory distress and pneumothorax in a neonate.
作者信息
Rana Nisha, Dalal Jagjit Singh, Lohchab Shamsher Singh, Singh Sandeep, Kumar Basant, Singh Sunita
机构信息
Department of Neonatology, Pt. B. D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryana India.
Department of Cardiothoracic and Vascular Surgery, Pt. B. D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, 124001 Haryana India.
出版信息
Indian J Thorac Cardiovasc Surg. 2023 Jul;39(4):417-420. doi: 10.1007/s12055-023-01510-x. Epub 2023 May 3.
UNLABELLED
Congenital pulmonary airway malformation (CPAM) is congenital pulmonary anomaly characterized by multicystic areas, over-distension, and proliferation of terminal bronchioles with lack of normal alveoli. Clinical presentation may vary from mild respiratory symptoms to severe respiratory distress and frequent pneumothoraxes. We report a rare case of neonatal CPAM type I manifested with neonatal respiratory distress and pneumothorax, which was managed successfully with left lower lobectomy.
SUPPLEMENTARY INFORMATION
The online version contains supplementary material available at 10.1007/s12055-023-01510-x.
未标注
先天性肺气道畸形（CPAM）是一种先天性肺部异常，其特征为多囊肿区域、过度扩张以及终末细支气管增殖，且缺乏正常肺泡。临床表现可能从轻微呼吸道症状到严重呼吸窘迫及频繁气胸不等。我们报告一例罕见的I型新生儿CPAM，表现为新生儿呼吸窘迫和气胸，通过左下肺叶切除术成功治疗。
补充信息
在线版本包含可在10.1007/s12055-023-01510-x获取的补充材料。
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