Key result
Surgical resection of a giant mediastinal teratoma achieves complete pulmonary re-expansion in a pediatric case.
Why the study?
Giant mediastinal teratomas in children are uncommon and cause significant intrathoracic compression, with limited pediatric literature available.
Case Report (n=1)
Surgical resection of a giant mediastinal teratoma in a pediatric patient can lead to complete pulmonary re-expansion and resolution of compressive symptoms.
Consider giant mediastinal teratoma in pediatric progressive dyspnea with thoracic widening; leaves open optimal timing and approach for resection.
Giant mediastinal teratomas in the pediatric population are uncommon entities that may grow insidiously and cause significant compression of intrathoracic structures. We report the case of a 10‐year‐old girl with a two‐year history of progressive exertional dyspnea, chest pain, orthopnea, and increasing thoracic enlargement. Chest radiography demonstrated marked mediastinal widening, and contrast‐enhanced chest CT revealed a predominantly cystic mediastinal mass measuring approximately 15 × 14 cm, with mediastinal shift and ipsilateral lung collapse. Routine laboratory tests were within normal limits, and surgical resection confirmed a mature mediastinal teratoma. The patient had an uneventful postoperative course, and follow‐up CT showed complete pulmonary re‐expansion with no residual lesion. This case highlights the clinical and imaging features that should raise suspicion for a giant mediastinal teratoma in children and underscores the importance of reporting these cases given the limited pediatric literature available.
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Lopez et al. (2026) conducted a case report in Giant mediastinal teratoma (n=1). Surgical resection was evaluated. Surgical resection of a 15 × 14 cm giant mediastinal teratoma in a 10-year-old girl resulted in complete pulmonary re-expansion with no residual lesion.
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