Mediastinal epithelioid haemangioendothelioma: A rare mediastinal tumour

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Abstract

We report the case of a 35-year-old patient with an incidental finding of an asymptomatic large (9.5 cm in diameter) anterior mediastinal tumour. Radiological findings favoured the diagnosis of a benign mediastinal teratoma. During surgical resection, we found a tumour adhering to the surrounding tissues, and encompassing the innominate vein which was totally occluded. Total tumoural exeresis was performed as well as the double cross-section of the innominate vein. Postoperatively, there was no left upper limb swelling, probably because of a chronic occlusion of the innominate vein. The hospital stay was uneventful. Immunohistochemistry diagnosed a mediastinal 'epithelioid haemangioendothelioma', which is a tumour of vascular origin. We believe that the tumour took origin from the innominate vein and invaded the anterior mediastinum. After a simple radiological follow-up, the patient is in complete remission 30 months after the operation. We present the case of this patient with the iconography, along with a review of the available literature concerning mediastinal epithelioid haemangioendotheliomas. © 2010 Published by European Association for Cardio-Thoracic Surgery. All rights reserved.

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Mansour, Z., Neuville, A., & Massard, G. (2010). Mediastinal epithelioid haemangioendothelioma: A rare mediastinal tumour. Interactive Cardiovascular and Thoracic Surgery, 10(1), 122–124. https://doi.org/10.1510/icvts.2009.216978

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