Adenomatoid Tumor of the Pericardium: A Case Report and Literature Review
Mokhtar H Abdelhammed, Nisha S Ramani

TL;DR
This paper reports a rare case of a benign tumor in the pericardium, adding to limited knowledge about such tumors in non-genital areas.
Contribution
The paper presents the second documented case of a pericardial adenomatoid tumor, expanding understanding of its rare thoracic occurrence.
Findings
A pericardial nodule was found incidentally during surgery in a 65-year-old male with no pericardial thickening.
Histopathology and immunohistochemistry confirmed mesothelial origin, excluding carcinoma and mesothelioma.
The tumor showed calretinin, D2-40, WT-1, and pan-cytokeratin positivity, with negative MOC-31 and BerEp4.
Abstract
Adenomatoid tumors (ATs) are rare benign neoplasms of mesothelial origin, commonly found in the genital tracts but occasionally reported in extragenital locations, including the thoracic cavity. We describe the second case of a pericardial AT in a 65-year-old male with multiple comorbidities, including end-stage renal disease, diabetes mellitus, and heart failure. A small pericardial nodule was incidentally discovered during coronary artery bypass graft surgery without any clinical evidence of pericardial thickening. Histopathologic evaluation showed a well-circumscribed nodule with solid nests of epithelioid to spindled cells with bland cytology within a fibrous stroma. Immunohistochemical analysis demonstrated strong and diffuse positivity for calretinin, D2-40, WT-1, and pan-cytokeratin, confirming mesothelial differentiation. Markers of epithelial origin like MOC-31 and BerEp4 were…
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Taxonomy
TopicsCardiac tumors and thrombi · Myasthenia Gravis and Thymoma · Adrenal and Paraganglionic Tumors
