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Updated: Sep 27, 2026

Thoracoscopic Extended Right Middle Plus Lower Sleeve Lobectomy for Non-Small-Cell Lung Cancer
Published on: February 27, 2026
[Bronchial mucoepidermoid carcinoma]
J I Bregante1, B Rituerto, F Font de Mora
1Servicio de Cirugía Pediátrica, Hospital Infantil Son Dureta, Palma de Mallorca.
Insights
This case study details a pediatric mucoepidermoid bronchial tumor, successfully treated with lobectomy. The young patient recovered well, showing no tumor recurrence and maintaining adequate breathing capacity post-surgery.
Area of Science:
- Pediatric Oncology
- Thoracic Surgery
Background:
- Lung tumors are rare in children, with mucoepidermoid bronchial tumors being an infrequent occurrence.
- Early diagnosis and appropriate treatment are crucial for favorable outcomes in pediatric lung cancer.
Observation:
- A seven-year-old boy presented with persistent fever and atelectasis, unresponsive to antibiotics.
- Bronchoscopy revealed a polypoid mass obstructing the right main bronchus, diagnosed as low-grade epidermoid carcinoma.
- Surgical intervention involved a right lower lobectomy and hilar adenopathy removal.
Findings:
- Post-operative follow-up showed granulation tissue, not tumor recurrence.
- Twelve months after surgery, the patient exhibited good health with no signs of relapse.
- Pulmonary function tests indicated an obstructive restrictive pattern, despite adequate breathing capacity.
Implications:
- This case highlights the possibility of successful surgical management of pediatric bronchial tumors.
- Conservative surgical approaches like bronchoplasty should be considered to minimize lung sequelae when feasible.
- Low-grade malignancy in pediatric lung tumors generally correlates with a positive prognosis.
Abstract:
We submit the case of a child afflicted with a mucoepidermoid bronchial tumor. The patient is a boy, aged seven, who after undergoing antibiotic treatment for six weeks because of a fever and atelectasia-condensation in the right lower lobe showed no signs of clinical improvement and was sent to our department to undergo further study and treatment. A bronchoscopy performed shows a polypoid mass that partially blocks the main bronchial tube a few milimiters under the access to the right upper lobe. A biopsy is carried out and the anatomopathological test shows there is a low degree epidermoid carcinoma. We decide to perform a lobectomy which for the tumor location and the lung condition has to be medium and lower right. We proceed to remove the adenopaty of hilium not affected by the tumor. The postoperative period develops without incidents. A check-up bronchoscopy performed three months later shows two polypoid masses in the right bronchial tube which, once a biopsy is performed, proved to be granulation tissue. Twelve months after undergoing surgery, the patient's condition is good, there is no evidence of tumor relapse and the breathing capacity is adequate, though there is an obstructive restrictive pattern in the espirometry. Even taking into consideration that lung tumors are extremely unusual, the epidermoid carcinoma is the one which most frequently occurs. The tumor's low malignancy is a sign that points to a good prognosis. Performing conservative surgery by means of bronchoplasty should be taken into account so as to keep the sequelae on the lung condition to a minimum, even though in this case the tumor location made it impossible.
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