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Thoracoscopic excision of an intrathoracic mesothelial cyst in a child
Bindi J Naik-Mathuria1, Ronald T Cotton, Megan E Fitch
1Division of Pediatric Surgery, Michael E DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX 77030, USA.
Insights
A rare intrathoracic mesothelial cyst in a child was successfully removed using minimally invasive thoracoscopic surgery. This approach offers a safe and effective treatment for these uncommon pediatric mediastinal masses.
Area of Science:
- Pediatric Surgery
- Thoracic Surgery
- Medical Case Reports
Background:
- Mesothelial cysts are rare, benign lesions lined by mesothelial cells, typically found near serous membranes.
- Intrathoracic mesothelial cysts are exceptionally uncommon in children, with fewer than 10 cases documented, often originating from the diaphragm.
Observation:
- An asymptomatic 5-year-old female presented with an incidentally discovered left-sided mediastinal mass on chest radiography.
- Magnetic resonance imaging revealed a hypodense, nonenhancing lesion in the left paravertebral region.
Findings:
- Video-assisted thoracoscopy facilitated the diagnosis and complete excision of the thin-walled, unilocular cyst.
- Histopathology confirmed a benign mesothelial cyst, positive for cytokeratin.
Implications:
- Mediastinal mesothelial cysts are exceedingly rare in pediatric patients.
- Minimally invasive thoracoscopic resection is a suitable and effective treatment for pediatric intrathoracic mesothelial cysts.
Purpose:
The aim of this study was to highlight the unique case of an intrathoracic mesothelial cyst in a 5-year-old child that was treated with a thoracoscopic resection.
Background:
Mesothelial cysts are benign cysts lined by a single layer of mesothelial cells. These rare lesions can be found on, or adjacent to, serous membranes but are only occasionally located within the thorax. In children, less than 10 intrathoracic cases have been described thus far, most of which are diaphragmatic in origin.
Case:
An asymptomatic 5-year-old female presented with a left-sided mediastinal mass incidentally discovered on a chest radiograph during a work-up for scoliosis. Magnetic resonance imaging demonstrated a hypodense, nonenhancing lesion measuring 3 x 2.5 x 8 cm in the left paravertebral region. Video-assisted thoracoscopy was employed for diagnosis and excision. The thin-walled cyst was dissected free from the pleura and completely excised thoracoscopically. Histopathology showed a benign, unilocular cyst lined with a cuboidal mesothelium that stained strongly positive for cytokeratin.
Conclusion:
Mediastinal mesothelial cysts have very rarely been reported in the pediatric population. In the case presented, the benign cyst was easily excised by using a minimally invasive thoracoscopic approach. Given the appropriate indications, we feel that thoracoscopic resection is well suited for such cases.
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