The First Reported Pediatric Case of Primary Myoepithelial Carcinoma Involving the Whole Lung: Surgical Radical Treatment and Prosthesis Implant.

IF 0.6 Q4 SURGERY
Claudia Filisetti, Tiziana Russo, Andrea Pansini, Claudio Vella, Camilla Viglio, Giovanna Riccipetitoni
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引用次数: 1

Abstract

Primary myoepithelial carcinoma of the lung (PMC-L) arising from the bronchial glands in lower respiratory tract is exceedingly rare. Thus far, few cases in adults and only one in a pediatric patient have been recorded. To our knowledge, this is the first report of PMC-L successfully removed in a child, focusing on the importance of multidisciplinary primary surgery for the treatment of this tumor. A 7-year-old girl was admitted for persistent cough and fever; she was unresponsive to oral antibiotics. Chest radiography showed loss of volume of left lung sustained by almost total atelectasis. After routine clinical investigations, she was referred for computed tomography scan and magnetic resonance imaging that documented the presence of a mass occupying the entire left upper lobe, infiltrating the pulmonary hilum (main bronchus, pulmonary artery, superior pulmonary vein, and pericardium). After multidisciplinary evaluation, the histopathologic diagnosis of PMC-L was established using ultrasonography-guided transthoracic core needle biopsy and bronchoscopic biopsies. She was then subjected to left pneumonectomy under extracorporeal circulation and positioning of a thoracic expander filled with 200 mL of saline solution. The postoperative course was uneventful. With TREP (very Rare Tumor in Pediatric Age) consent radiotherapy was performed (61.2 Gy). At the 10-month follow-up, the patient was alive, breathing normally without any oxygen support, without recurrence of PMC-L or metastasis, and without any chest deformity. To our knowledge, this is the first case where a pediatric patient was successfully operated for PMC-L involving the whole lung. Extracorporeal circulation enabled us to perform radical primary surgery. Prosthesis implant not only maintained normal chest expansion but also allowed focused radiotherapy, thus enabling us to prevent damage to vital organs.

Abstract Image

Abstract Image

首例小儿原发性肌上皮癌累及全肺:手术根治及假体植入。
原发性肺肌上皮癌(PMC-L)起源于下呼吸道的支气管腺是非常罕见的。到目前为止,成人病例很少,儿科患者只有一例。据我们所知,这是首个在儿童中成功切除PMC-L的报道,强调了多学科基础手术对治疗该肿瘤的重要性。一名7岁女孩因持续咳嗽和发烧入院;口服抗生素对她没有反应。胸片显示左肺容量减少,几乎完全肺不张。常规临床检查后,患者接受计算机断层扫描和磁共振成像检查,发现肿块占据整个左上肺叶,浸润肺门(主支气管、肺动脉、上肺静脉和心包)。经多学科评估,采用超声引导下经胸穿刺活检和支气管镜活检建立PMC-L的组织病理学诊断。然后在体外循环下行左侧全肺切除术,胸腔扩张器置入200 mL生理盐水。术后过程平淡无奇。对TREP(儿童年龄非常罕见的肿瘤)进行同意放疗(61.2 Gy)。随访10个月,患者存活,呼吸正常,无氧支持,无PMC-L复发或转移,无胸部畸形。据我们所知,这是第一例小儿全肺PMC-L手术成功的病例。体外循环使我们能够进行根治性初级手术。假体植入不仅可以维持正常的胸部扩张,还可以进行聚焦放疗,从而使我们能够防止对重要器官的损害。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
33.30%
发文量
39
审稿时长
12 weeks
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