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Mediastinal seminoma presenting with superior vena cava syndrome. | LitMetric

Mediastinal seminoma presenting with superior vena cava syndrome.

BMJ Case Rep

Division of General Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Published: June 2017

AI Article Synopsis

  • A 31-year-old male with no prior health issues developed superior vena cava syndrome, raising suspicion of malignancy due to unexplained weight loss and childhood radiation exposure.
  • A large anterior mediastinal mass was diagnosed as an extragonadal seminoma, a rare tumor known to be linked to cardiac and pulmonary complications, particularly in patients with a history of radiation exposure.
  • After starting chemotherapy, the patient faced complications from blood clots, but responded well to anticoagulation treatment and remains cancer-free 72 months post-therapy without requiring surgery.

Article Abstract

We present a rare cause of superior vena cava syndrome (SVC) in a previously healthy male aged 31 years. Malignancy was suspected due to unintentional weight loss and childhood exposure to radioactive fallout from a nuclear facility accident. A very large anterior mediastinal mass was identified and demonstrated to be an extragonadal seminoma. Extragonadal germ cell tumours are rare tumours with a high potential for cardiovascular, pulmonary and vascular sequelae. Studies have documented an increased risk of developing seminoma in patients with radioactive exposure. Chemotherapy was initiated, during which the patient experienced progressive and new symptoms, found to be due to extensive thromboembolic disease, which responded well to anticoagulation. Seventy-two months after completing chemotherapy, without need for surgical management, he remains free of the disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534895PMC
http://dx.doi.org/10.1136/bcr-2016-218282DOI Listing

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