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Published on: January 19, 2019
[Primary Pulmonary Tumor in an Adolescent]
Luís Rodrigues1, Rui Domingues2, Diana Amaral2
1Unidade de Pneumologia Pediátrica. Área da Mulher, da Criança e do Adolescente. Hospital Dona Estefânia. Centro Hospitalar Universitário de Lisboa Central. Lisboa; Serviço de Pediatria. Departamento da Saúde da Mulher e da Criança. Hospital do Espírito Santo de Évora. Évora. Portugal.
Pediatric inflammatory myofibroblastic tumors of the lung are rare and challenging to diagnose. Early detection and surgical resection led to a full recovery in a 15-year-old patient.
Area of Science:
- Pediatric Oncology
- Thoracic Surgery
- Pulmonology
Background:
- Primary lung tumors in children are uncommon, exhibiting diverse histology and treatment strategies.
- Inflammatory myofibroblastic tumors (IMT) of the lung represent a rare entity, typically affecting younger individuals, with unknown etiology.
- Diagnostic challenges arise from variable clinical presentations and radiological findings.
Observation:
- A 15-year-old adolescent presented with a solitary pulmonary nodule detected on chest radiography during a respiratory infection.
- Diagnostic investigations confirmed the presence of an inflammatory myofibroblastic tumor of the lung.
- The patient underwent atypical resection via video-assisted thoracoscopic surgery.
Findings:
- Surgical intervention resulted in complete recovery for the adolescent.
- This case underscores the rarity of pulmonary IMT in pediatric patients.
- A high index of suspicion is crucial for timely diagnosis.
Implications:
- Highlights the importance of comprehensive etiological investigation for pulmonary nodules in adolescents.
- Demonstrates the efficacy of minimally invasive surgical techniques for pediatric lung tumors.
- Emphasizes the need for increased awareness of rare pediatric lung neoplasms among clinicians.
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