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肺胸膜胚细胞瘤伪装为气胸的室间隔缺损患者。

Pleuropulmonary blastoma masquerading as pneumothorax in a patient with a ventricular septal defect.

机构信息

Department of Cardiothoracic and Vascular Surgery, 28730All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.

出版信息

Asian Cardiovasc Thorac Ann. 2022 Oct;30(8):939-942. doi: 10.1177/02184923221113297. Epub 2022 Jul 27.

Abstract

Pleuropulmonary blastoma is a rare pediatric primary lung tumor. We report a case of a child with Down syndrome and a large ventricular septal defect presenting with pleuropulmonary blastoma initially misdiagnosed as spontaneous pneumothorax. Following tube thoracostomy drainage of the pneumothorax, the child underwent surgical closure of the ventricular septal defect. However, the postoperative period was complicated by recurrent left pleural collection requiring prolonged intercostal tube drainage and two thoracotomies to evacuate the necrotic pleural material. The biopsy of the necrotic material was suggestive of type III pleuropulmonary blastoma. In view of the high propensity of metastasis associated with this variant of a tumor, the patient was started on chemotherapy. This case report highlights the possibility of pleuropulmonary blastoma presenting as pneumothorax and emphasizes the need to consider the etiology, before intervening in a child presenting with spontaneous pneumothorax.

摘要

肺胸膜胚细胞瘤是一种罕见的小儿原发性肺肿瘤。我们报告了一例唐氏综合征患儿,伴有巨大室间隔缺损,最初被误诊为自发性气胸,表现为肺胸膜胚细胞瘤。在对气胸进行胸腔引流管引流后,患儿接受了室间隔缺损的手术修复。然而,术后期间出现左侧胸腔反复积液,需要长时间肋间管引流和两次开胸手术以清除坏死的胸膜物质。坏死物质的活检提示为 III 型肺胸膜胚细胞瘤。鉴于这种肿瘤类型转移的高倾向性,患儿开始接受化疗。本病例报告强调了肺胸膜胚细胞瘤表现为气胸的可能性,并强调在对自发性气胸患儿进行干预之前,需要考虑病因。

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