Congenital Cystic Adenomatoid Malformation: A Case Report with Clinical, Radiological, Histological, and Surgical Features

作     者：Karim Lahrache Samia Malki Soulaimane M’harzi Anas Ayyad Sahar Messouadi Houssain Benhaddou Amal Bennani Rim Amrani Karim Lahrache;Samia Malki;Soulaimane M’harzi;Anas Ayyad;Sahar Messouadi;Houssain Benhaddou;Amal Bennani;Rim Amrani

作者机构：Faculty of Medicine and Pharmacy of Oujda Mohammed I University of Oujda Oujda Morocco Department of Neonatology and Neonatal Reanimation Mohammed VI University Hospital of Oujda Oujda Morocco Anatomopathology Department Mohammed VI University Hospital of Oujda Oujda Morocco Paediatric Surgery Department Mohammed VI University Hospital of Oujda Oujda Morocco 

出 版 物：《Open Journal of Pediatrics》 (儿科学期刊（英文）)

年 卷 期：2023年第13卷第4期

页      面：465-472页

学科分类：1002[医学-临床医学] 100214[医学-肿瘤学] 10[医学] 

主　　题：Congenital Cystic Adenomatoid Malformation Congenital Disorder Lung Respiratory Distress Newborn 

摘      要：Background: Congenital cystic adenomatoid malformation (CCAM) is a congenital anomaly of lung development, accounting for approximately 25% of congenital lung lesions. Respiratory distress often occurs during the neonatal period, and in 80% to 85% of cases, the diagnosis is made before the age of 2 years following respiratory infections. Case Report: We report a case of MAKC diagnosed in the neonatal period. The diagnosis was based on clinical, radiological and histological elements. Our patient underwent surgical resection. Histological examination confirmed the diagnosis of MAKC without any sign of malignancy. The postoperative evolution was good. Conclusion: Clinicians and pathologists should recognize the early discovery of MAKC in neonatal age. The clinical diagnosis strongly guided by the radiological approach is confirmed by the pathological anatomy insofar as the therapeutic sanction is surgical in the majority of the cases.