Basa Mihail, Mitrovic Nemanja, Aleksic Dragana, Samardzija Gordana, Stajevic Mila, Dizdarevic Ivan, Dencic Fekete Marija, Grba Tijana, Sovtic Aleksandar
Department of Pulmonology, Mother and Child Health Care Institute of Serbia, 11070 Beograd, Serbia.
Pathology Department, Mother and Child Health Care Institute of Serbia, 11070 Beograd, Serbia.
Biomedicines. 2025 Jul 25;13(8):1824. doi: 10.3390/biomedicines13081824.
: Primary malignant lung tumors in children are rare and diagnostically challenging. This study presents a single-center experience in the diagnosis and treatment of these tumors, emphasizing the role of histopathological and genetic profiling in informing individualized therapeutic strategies. : We retrospectively reviewed records of seven pediatric patients (ages 2-18) treated from 2015 to 2025. Diagnostics included laboratory tests, chest CT, bronchoscopy, and histopathological/immunohistochemical analysis. Treatment primarily involved surgical resection, complemented by chemo-, radio-, or targeted therapies when indicated. : Inflammatory myofibroblastic tumor (IMT) represented the most commonly diagnosed entity (3/7 cases). The tumors presented with nonspecific symptoms, most frequently dry cough. Tumor type distribution was age-dependent, with aggressive forms such as pleuropulmonary blastoma predominantly affecting younger children, whereas IMT and carcinoid tumors were more common in older patients. Surgical resection remained the mainstay of treatment in the majority of cases. Bronchoscopy served as a valuable adjunct in the initial management of tumors exhibiting intraluminal growth, allowing for direct visualization, tissue sampling, and partial debulking to alleviate airway obstruction. In patients with an initially unresectable IMT harboring specific gene fusion rearrangement (e.g., TFG::ROS1), neoadjuvant targeted therapy with crizotinib enabled adequate tumor shrinkage to allow for subsequent surgical resection. Two patients in the study cohort died as a result of disease progression. : A multidisciplinary diagnostic approach-integrating radiologic, bronchoscopic, histopathological, and genetic evaluations-ensures high diagnostic accuracy. While conventional treatments remain curative in many cases, targeted therapies directed at specific molecular alterations may offer essential therapeutic options for selected patients.
儿童原发性恶性肺肿瘤较为罕见,诊断具有挑战性。本研究介绍了单中心对这些肿瘤的诊断和治疗经验,强调组织病理学和基因谱分析在制定个体化治疗策略中的作用。
我们回顾性分析了2015年至2025年期间接受治疗的7例儿科患者(年龄2 - 18岁)的记录。诊断方法包括实验室检查、胸部CT、支气管镜检查以及组织病理学/免疫组织化学分析。治疗主要包括手术切除,必要时辅以化疗、放疗或靶向治疗。
炎性肌纤维母细胞瘤(IMT)是最常见的诊断类型(3/7例)。这些肿瘤表现为非特异性症状,最常见的是干咳。肿瘤类型分布与年龄有关,侵袭性形式如胸膜肺母细胞瘤主要影响年幼儿童,而IMT和类癌肿瘤在年长患者中更为常见。在大多数病例中,手术切除仍然是主要的治疗方法。支气管镜检查在腔内生长肿瘤的初始管理中是一种有价值的辅助手段,可直接观察、组织取样并部分减瘤以缓解气道阻塞。对于最初无法切除但存在特定基因融合重排(如TFG::ROS1)的IMT患者,使用克唑替尼进行新辅助靶向治疗可使肿瘤充分缩小,以便随后进行手术切除。研究队列中有2例患者因疾病进展死亡。
多学科诊断方法——整合放射学、支气管镜、组织病理学和基因评估——可确保高诊断准确性。虽然传统治疗在许多情况下仍然可以治愈,但针对特定分子改变的靶向治疗可能为选定患者提供重要的治疗选择。