Primary Lung Tumors in Children: Insights from a Single-Center Case Series

<b>Background</b>: Primary lung tumors in pediatric patients are rare, predominantly malignant, and present diagnostic challenges due to symptom overlap with more common conditions such as inflammatory processes or asthma. Evidence-based approaches for managing these rare neoplasms in childhood are scarce. This retrospective study reports the experience of a pediatric referral center in diagnosing and treating these tumors. <b>Methods:</b> Pediatric primary lung tumors treated at Giannina Gaslini Children's Hospital between January 2016 and January 2024 were included. Data on clinical presentation, histopathology, imaging, treatment approaches, and outcomes were systematically collected and analyzed. <b>Results:</b> Nine patients (six males and three females) were identified, with a mean age (±SD) at diagnosis of 8.81 ± 5 years. The most common clinical manifestation was recurrent pneumonia (four patients), followed by persistent cough and wheezing (three patients). The average duration of symptoms before diagnosis was 12.8 months ± 12.2 months. Histopathological diagnoses were typical carcinoid tumors (<i>n</i> = 2), atypical carcinoid tumors (<i>n</i> = 2), inflammatory myofibroblastic tumors (<i>n</i> = 2), congenital peribronchial myofibroblastic tumor (<i>n</i> = 1), myoepithelial carcinoma (<i>n</i> = 1), and pleuropulmonary blastoma (<i>n</i> = 1). Radical surgery resulted in complete response for seven patients, with a median follow-up of 52 months (IQR 39 months). The myoepithelial carcinoma was treated with multimodal therapy, relapsed after 17 months, and adjuvant chemotherapy is currently ongoing. Neoadjuvant chemotherapy for the pleuropulmonary blastoma is currently ongoing. <b>Conclusions:</b> Primary lung tumors in children, though rare, may have favorable outcomes when appropriately managed. Nonspecific clinical presentations often contribute to diagnostic delays. This study highlights the critical need of thorough evaluation in cases of persistent, therapy-resistant aspecific respiratory symptoms. Early diagnosis, coupled with complete surgical resection, significantly improves prognosis.

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Journal
Journal of Clinical Medicine
Published
2025-03-22
DOI
https://doi.org/10.3390/jcm14072173
Citations
4
Primary Topic
Congenital Diaphragmatic Hernia Studies
Type
article
Field-Weighted Citation Impact
8.03
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article

Primary Lung Tumors in Children: Insights from a Single-Center Case Series

Lorenzo Anfigeno, Paola Borgia, Angelo Florio, Francesca Buffelli et al.
4 citations
Journal of Clinical Medicine
Congenital Diaphragmatic Hernia Studies
8.03
article

Primary Lung Tumors in Children: Insights from a Single-Center Case Series

Lorenzo Anfigeno, Paola Borgia, Angelo Florio, Francesca Buffelli, Giovanni Arturo Rossi, Michele Torre, Teresa Battaglia, Barbara Cafferata, Virginia Livellara, Pietro Salvati, C. Paratore, Maria Beatrice Damasio, Massimo Conte, Annalisa Gallizia, Alberto Garaventa, Valerio Gaetano Vellone, Oliviero Sacco, Katia Perri, Alessio Conte, Francesca Rizzo, Carlo Castellani, Marco Del Monte
article en
4 citations

Abstract

<b>Background</b>: Primary lung tumors in pediatric patients are rare, predominantly malignant, and present diagnostic challenges due to symptom overlap with more common conditions such as inflammatory processes or asthma. Evidence-based approaches for managing these rare neoplasms in childhood are scarce. This retrospective study reports the experience of a pediatric referral center in diagnosing and treating these tumors. <b>Methods:</b> Pediatric primary lung tumors treated at Giannina Gaslini Children's Hospital between January 2016 and January 2024 were included. Data on clinical presentation, histopathology, imaging, treatment approaches, and outcomes were systematically collected and analyzed. <b>Results:</b> Nine patients (six males and three females) were identified, with a mean age (±SD) at diagnosis of 8.81 ± 5 years. The most common clinical manifestation was recurrent pneumonia (four patients), followed by persistent cough and wheezing (three patients). The average duration of symptoms before diagnosis was 12.8 months ± 12.2 months. Histopathological diagnoses were typical carcinoid tumors (<i>n</i> = 2), atypical carcinoid tumors (<i>n</i> = 2), inflammatory myofibroblastic tumors (<i>n</i> = 2), congenital peribronchial myofibroblastic tumor (<i>n</i> = 1), myoepithelial carcinoma (<i>n</i> = 1), and pleuropulmonary blastoma (<i>n</i> = 1). Radical surgery resulted in complete response for seven patients, with a median follow-up of 52 months (IQR 39 months). The myoepithelial carcinoma was treated with multimodal therapy, relapsed after 17 months, and adjuvant chemotherapy is currently ongoing. Neoadjuvant chemotherapy for the pleuropulmonary blastoma is currently ongoing. <b>Conclusions:</b> Primary lung tumors in children, though rare, may have favorable outcomes when appropriately managed. Nonspecific clinical presentations often contribute to diagnostic delays. This study highlights the critical need of thorough evaluation in cases of persistent, therapy-resistant aspecific respiratory symptoms. Early diagnosis, coupled with complete surgical resection, significantly improves prognosis.

Journal of Clinical MedicineVol. 14(7)
Istituto Giannina Gaslini (IT), Istituti di Ricovero e Cura a Carattere Scientifico (IT), University of Genoa (IT)
Openalex Percentile: Top 3%
Congenital Diaphragmatic Hernia Studies
8.03
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