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Primary Mediastinal Neuroendocrine Tumor: A Case of Atypical Carcinoid
Konstantinos Kosmas1, Ioannis Vamvakaris2, Eirini Klapsinou3
1Cytology Department, General Hospital of Thoracic Diseases of Athens "Sotiria", Athens, GRC.
Abstract:
Primary mediastinal neuroendocrine tumor (PMNET) is an extremely rare clinical entity and few cases have been described in the literature. Here, we report a histologically confirmed rare PMNET case of a 66-year-old male patient with a mass detected in the anterior upper mediastinum by chest high-resolution computed tomography (HRCT). Early detection and surgical intervention of this neoplasm are critical for long term survival, though the tumor is associated with a dismal outcome.

