1例青少年颗粒细胞支气管源性肿瘤:罕见病例报告及文献复习。

IF 1.2 Q2 PEDIATRICS
Clinical Medicine Insights-Pediatrics Pub Date : 2025-09-09 eCollection Date: 2025-01-01 DOI:10.1177/11795565251366784
Irmak Tanal Şambel, Abdurrahman Erdem Başaran, Betül Bankoğlu Parlak, Didar Ağca Cengiz, İrem Hicran Özbudak, Ayşen Bingöl
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引用次数: 0

摘要

原发性肺肿瘤在儿科患者中很少见,良性类型比恶性类型更常见。来源于神经外胚层的颗粒细胞瘤(gct)在肺部并不常见,在儿童中尤其罕见。我们报告一例16岁的女性持续呼吸道症状最初诊断为哮喘,谁最终发现有支气管颗粒细胞瘤。经组织病理学证实,病变经刚性支气管镜切除。我们还提供了一个文献综述,重点是儿童肺部gct。对于持续呼吸道症状且药物治疗无反应的青少年,在鉴别诊断时应考虑颗粒细胞肿瘤。早期影像学检查和支气管镜检查有助于及时诊断和肺保留治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Adolescent With a Granular Cell Bronchogenic Tumor: A Rare Case Report and Review of the Literature.

Primary pulmonary tumors are rare in pediatric patients, and benign types are more frequently observed than malignant ones. Granular cell tumors (GCTs), of neuroectodermal origin, are uncommon in the lungs and especially rare in children. We report a case of a 16-year-old female with persistent respiratory symptoms initially diagnosed as asthma, who was ultimately found to have a bronchial granular cell tumor. The diagnosis was confirmed histopathologically, and the lesion was removed via rigid bronchoscopy. We also provide a review of the literature focusing on pediatric pulmonary GCTs. Granular cell tumors should be considered in the differential diagnosis of adolescents with persistent respiratory symptoms unresponsive to medical therapy. Early imaging and bronchoscopy can assist in timely diagnosis and lung-sparing treatment.

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