El Fakiri Karima, Draiss Ghizlane, Rada Noureddine, Bouskraoui Mohammed, Hamdaoui Abderrachid, Oulad Saiad Mohamed
Pediatric A Department, Pediatric Pulmonology Unit, Mother and Child Hospital, University Hospital Mohammed VI Marrakesh, Marrakesh, Morocco.
Pathology Laboratory Zohor El Hadika El Kobra Marrakesh, Marrakesh, Morocco.
Case Rep Pediatr. 2020 Sep 9;2020:8879661. doi: 10.1155/2020/8879661. eCollection 2020.
Pneumoblastoma is a rare primary childhood tumor. We report the observation of an infant aged 2 years and 8 months who presented with dry cough and dyspnea. The physical examination found mixed pleural effusion syndrome on the right. The chest X-ray revealed a right pneumothorax. Biology has shown leukocytosis at 16,000/mm. The CT scan revealed parenchymal air cystic lesions affecting the outer segment of the middle lobe mimicking a pulmonary malformation. Thoracic drainage brought back 100 ml of the fluid. Two months later, when a pyopneumothorax appeared, a medium lobectomy was performed. Pathological study specimen showed a high-grade type II pneumoblastoma The extension assessment identified a secondary hepatic location. Chemotherapy has been indicated. This observation illustrates the diagnosis challenge of pneumoblastoma in children.
肺母细胞瘤是一种罕见的儿童原发性肿瘤。我们报告了一名2岁8个月大的婴儿,其表现为干咳和呼吸困难。体格检查发现右侧有混合性胸腔积液综合征。胸部X线显示右侧气胸。血液检查显示白细胞计数为16,000/mm³。CT扫描显示实质性气囊肿块,累及中叶外侧段,类似肺发育异常。胸腔引流引出100毫升液体。两个月后,当出现脓气胸时,进行了中叶切除术。病理研究标本显示为高级别II型肺母细胞瘤。扩展评估发现有肝脏转移。已开始化疗。该病例说明了儿童肺母细胞瘤的诊断挑战。