https://doi.org/10.4081/cdr.12.12119
Germ cell tumor impersonating as a pleuropericardial cyst: a rare phenomenon
Submitted: 22 November 2023
Accepted: 24 January 2024
Published: 31 January 2024
Accepted: 24 January 2024
Abstract Views: 304
PDF: 108
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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
A Mixed Germ Cell Tumor (MGCT) is a rare tumor with a low degree of differentiation. The most common sites are yolk sac and astrocytoma. Usually, it is gonadal, but in 5% of cases, it can present as extragonadal. The most common extragonadal site is the mediastinum, where the mediastinal mass sometimes mimics thymoma, lymphoma, pericardial cyst, and also occasionally causes pericardial tamponade. The presentations vary, ranging from accidental findings on routine radiography to life-threatening respiratory and cardiovascular compromission. We present an extragonadal MGCT case presenting as a mediastinal mass with symptoms of 1 year duration. The diagnosis was confirmed on Histopathological Examination (HPE) of surgically excised specimen. Given a possible life-threatening condition, a timely diagnosis is required.
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How to Cite
Pandey, G., Gupta, S., Singhal, P., Rizvi, S. H. M., Pandey, S., & Mishra, S. (2024). Germ cell tumor impersonating as a pleuropericardial cyst: a rare phenomenon. Chest Disease Reports, 12(1). https://doi.org/10.4081/cdr.12.12119
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