Xanthogranulomatous Oophoritis: A Rare Case Report
- PMID: 37727159
- PMCID: PMC10505683
- DOI: 10.7759/cureus.43724
Xanthogranulomatous Oophoritis: A Rare Case Report
Abstract
Xanthogranulomatous oophoritis is a rare, chronic and non-neoplastic condition in which a heavy foamy histiocyte inflammatory infiltrate admixed with neutrophils, plasma cells, multinucleated giant cells, fibroblasts and foci of necrosis causing extensive tissue damage and organ destruction. The gallbladder and kidney are just two examples of the different organs that exhibit histological changes resembling xanthogranulomatous alteration. The present case involved a 40-year-old female who presented with a tuboovarian mass and was ultimately diagnosed with xanthogranulomatous oophritis, despite initial clinicoradiological suspicions for malignancy. Xanthogranulomatous oophritis is a significant entity because, clinically and radiographically, it resembles tumours of the ovary and hinges on a careful histopathological analysis to establish a diagnosis.
Keywords: histiocytes; inflammation; macrophages; oophoritis; xanthogranulomatous.
Copyright © 2023, Dawande et al.
Conflict of interest statement
The authors have declared that no competing interests exist.
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