Document Type
Article
Department
Cardiothoracic Surgery
Abstract
Malignant germ cell tumours of the mediastinum are rare, presenting mostly in young males. These are bulky tumours, mostly intrathoracic, infiltrating into adjacent structures early in the growth process. Patients may present with symptoms of compression. Occasionally, mediastinal adenopathy and superior vena cava (SVC) syndrome may occur. We discuss a case of a 19 year old boy with six weeks history of progressively worsening shortness of breath and mid-sternal chest heaviness and one month history of swelling of the face and upper limbs. The entire face and upper extremities were grossly oedematous with engorged veins suggesting SVC syndrome. CT scan chest showed a large mediastinal mass 18 x 24 cm extending from the superior mediastinum to the mid pericardial area. The trachea was extrinsically compressed to almost 80% at its distal portion. Mass was resected completely. Post operative course was unremarkable. The final histopathology showed a fibrotic mass with no viable tumour. Surgery followed by radiation therapy has been the usual initial treatment with multimodal chemotherapy showing remarkable results.
Publication (Name of Journal)
Journal of the Pakistan Medical Association
Recommended Citation
Fatimi, S.,
Shahid, B.,
Hanif, H.,
Muzaffar, M.
(2010). Mediastinal seminoma presenting as superior vena cava syndrome and tracheal obstruction. Journal of the Pakistan Medical Association, 60(10), 861-2.
Available at:
https://ecommons.aku.edu/pakistan_fhs_mc_surg_cardiothoracic/15