Related Experiment Video
Updated: May 25, 2026

06:51
A Patient-Derived Xenograft Model for Venous Malformation
Published on: June 15, 2020
Bilateral Mediastinal Lymphangiohemangiomas Containing Anomalous Venous Components - A case report -
1Department of Thoracic and Cardiovascular Surgery, Daegu Catholic University Medical Center, Catholic University of Daegu, Korea.
The Korean Journal of Thoracic and Cardiovascular Surgery
|January 21, 2012
Summary
Bilateral lymphangiohemangiomas in the mediastinum are exceptionally rare. This case report details a successful surgical removal in a child, offering valuable insights into managing this uncommon condition.
Area of Science:
- Thoracic Surgery
- Pediatric Oncology
- Vascular Malformations
Background:
- Lymphangiohemangiomas are rare benign tumors, often presenting in the head, neck, or axilla.
- Mediastinal lymphangiohemangiomas are exceedingly rare, with limited published cases.
- Bilateral presentation of mediastinal lymphangiohemangiomas is exceptionally uncommon.
Observation:
- A 7-year-old boy presented with an incidental abnormal mediastinal shadow on chest X-ray.
- Chest CT revealed large masses in the left superior and right posterior mediastinum.
- Anomalous venous connections were identified: left mass to the left innominate vein, right mass to the left atrium.
Findings:
- Surgical excision of the left-sided mass was performed first, followed by the right-sided mass one month later.
- Careful dissection and ligation of anomalous venous channels were crucial during the procedures.
- The patient experienced no complications and showed no recurrence 30 months post-operation.
Implications:
- This case highlights the possibility of bilateral mediastinal lymphangiohemangiomas, a previously unreported occurrence.
- Successful surgical management demonstrates the feasibility of treating these rare bilateral malformations.
- The findings contribute to the limited literature on mediastinal lymphangiohemangiomas, aiding future diagnosis and treatment strategies.