Brooklynne A.S. Dilley-Maltenfort, John Roebel, Todd Boyd, Rachael Courtney, Daniel Evans, Anne Mackow
{"title":"青少年肺叶内肺隔离合并肺黏液表皮样癌1例","authors":"Brooklynne A.S. Dilley-Maltenfort, John Roebel, Todd Boyd, Rachael Courtney, Daniel Evans, Anne Mackow","doi":"10.1016/j.epsc.2025.103026","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Primary pulmonary carcinomas in children are exceedingly rare, representing only 0.2 of every 1,000,000 childhood cancer diagnoses. Approximately 9 % of them are pulmonary mucoepidermoid carcinoma (PMEC). Due to nonspecific symptoms that mimic common respiratory conditions, their diagnosis is often delayed.</div></div><div><h3>Case presentation</h3><div>A 17-year-old previously healthy male presented with fever, cough, and nasal congestion and was treated with antibiotics for presumed pneumonia. Despite completing treatment, his symptoms persisted. Over the following month, serial chest X-rays showed a persistent left lower lobe opacity with atelectasis. A chest computerized tomography (CT) revealed a 2.7-cm non-calcified mass in the left lower lobe with post-obstructive changes. He was admitted to our institution with worsening symptoms but improved on IV antibiotics and was discharged home shortly thereafter. We did a flexible bronchoscopy to investigate the calcified mass and found compression of the posterior basal segment bronchi. Samples of the bronchoalveolar lavage grew <em>Haemophilus influenzae</em>. Elective surgical resection was delayed due to insurance issues for several months. While awaiting clearance, he presented with an episode of hemoptysis, which resolved spontaneously. A repeat CT showed slight enlargement of the mass and worsening bronchiectasis. He underwent a video-assisted thoracoscopic left lower lobectomy during which we found a systemic vessel arising from the thoracic aorta, which confirmed the diagnosis of an intralobar pulmonary sequestration. The lobe containing the mass and the sequestration was completely removed. The pathology confirmed a <strong>low-</strong>grade pulmonary mucoepidermoid carcinoma (PMEC) within the intrapulmonary sequestration. The patient was discharged on postoperative day 3 and returned to normal activities without further respiratory symptoms. At 1 month of follow up he continues to be asymptomatic and remains under surveillance by the oncology team.</div></div><div><h3>Conclusion</h3><div>Children and adolescents with persistent respiratory symptoms require a comprehensive imaging workup to rule out pulmonary malignancies, which, although rare, can still occur in this population.</div></div>","PeriodicalId":45641,"journal":{"name":"Journal of Pediatric Surgery Case Reports","volume":"118 ","pages":"Article 103026"},"PeriodicalIF":0.2000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Intralobar pulmonary sequestration combined with pulmonary mucoepidermoid carcinoma in an adolescent: A case report\",\"authors\":\"Brooklynne A.S. Dilley-Maltenfort, John Roebel, Todd Boyd, Rachael Courtney, Daniel Evans, Anne Mackow\",\"doi\":\"10.1016/j.epsc.2025.103026\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><div>Primary pulmonary carcinomas in children are exceedingly rare, representing only 0.2 of every 1,000,000 childhood cancer diagnoses. Approximately 9 % of them are pulmonary mucoepidermoid carcinoma (PMEC). Due to nonspecific symptoms that mimic common respiratory conditions, their diagnosis is often delayed.</div></div><div><h3>Case presentation</h3><div>A 17-year-old previously healthy male presented with fever, cough, and nasal congestion and was treated with antibiotics for presumed pneumonia. Despite completing treatment, his symptoms persisted. Over the following month, serial chest X-rays showed a persistent left lower lobe opacity with atelectasis. A chest computerized tomography (CT) revealed a 2.7-cm non-calcified mass in the left lower lobe with post-obstructive changes. He was admitted to our institution with worsening symptoms but improved on IV antibiotics and was discharged home shortly thereafter. We did a flexible bronchoscopy to investigate the calcified mass and found compression of the posterior basal segment bronchi. Samples of the bronchoalveolar lavage grew <em>Haemophilus influenzae</em>. Elective surgical resection was delayed due to insurance issues for several months. While awaiting clearance, he presented with an episode of hemoptysis, which resolved spontaneously. A repeat CT showed slight enlargement of the mass and worsening bronchiectasis. He underwent a video-assisted thoracoscopic left lower lobectomy during which we found a systemic vessel arising from the thoracic aorta, which confirmed the diagnosis of an intralobar pulmonary sequestration. The lobe containing the mass and the sequestration was completely removed. The pathology confirmed a <strong>low-</strong>grade pulmonary mucoepidermoid carcinoma (PMEC) within the intrapulmonary sequestration. The patient was discharged on postoperative day 3 and returned to normal activities without further respiratory symptoms. At 1 month of follow up he continues to be asymptomatic and remains under surveillance by the oncology team.</div></div><div><h3>Conclusion</h3><div>Children and adolescents with persistent respiratory symptoms require a comprehensive imaging workup to rule out pulmonary malignancies, which, although rare, can still occur in this population.</div></div>\",\"PeriodicalId\":45641,\"journal\":{\"name\":\"Journal of Pediatric Surgery Case Reports\",\"volume\":\"118 \",\"pages\":\"Article 103026\"},\"PeriodicalIF\":0.2000,\"publicationDate\":\"2025-04-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pediatric Surgery Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2213576625000715\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"PEDIATRICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Surgery Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213576625000715","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PEDIATRICS","Score":null,"Total":0}
Intralobar pulmonary sequestration combined with pulmonary mucoepidermoid carcinoma in an adolescent: A case report
Introduction
Primary pulmonary carcinomas in children are exceedingly rare, representing only 0.2 of every 1,000,000 childhood cancer diagnoses. Approximately 9 % of them are pulmonary mucoepidermoid carcinoma (PMEC). Due to nonspecific symptoms that mimic common respiratory conditions, their diagnosis is often delayed.
Case presentation
A 17-year-old previously healthy male presented with fever, cough, and nasal congestion and was treated with antibiotics for presumed pneumonia. Despite completing treatment, his symptoms persisted. Over the following month, serial chest X-rays showed a persistent left lower lobe opacity with atelectasis. A chest computerized tomography (CT) revealed a 2.7-cm non-calcified mass in the left lower lobe with post-obstructive changes. He was admitted to our institution with worsening symptoms but improved on IV antibiotics and was discharged home shortly thereafter. We did a flexible bronchoscopy to investigate the calcified mass and found compression of the posterior basal segment bronchi. Samples of the bronchoalveolar lavage grew Haemophilus influenzae. Elective surgical resection was delayed due to insurance issues for several months. While awaiting clearance, he presented with an episode of hemoptysis, which resolved spontaneously. A repeat CT showed slight enlargement of the mass and worsening bronchiectasis. He underwent a video-assisted thoracoscopic left lower lobectomy during which we found a systemic vessel arising from the thoracic aorta, which confirmed the diagnosis of an intralobar pulmonary sequestration. The lobe containing the mass and the sequestration was completely removed. The pathology confirmed a low-grade pulmonary mucoepidermoid carcinoma (PMEC) within the intrapulmonary sequestration. The patient was discharged on postoperative day 3 and returned to normal activities without further respiratory symptoms. At 1 month of follow up he continues to be asymptomatic and remains under surveillance by the oncology team.
Conclusion
Children and adolescents with persistent respiratory symptoms require a comprehensive imaging workup to rule out pulmonary malignancies, which, although rare, can still occur in this population.