Xanthogranulomatous Oophoritis: A Rare and Forgotten Entity
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This case report describes a 25-year-old woman with xanthogranulomatous oophoritis, a rare inflammatory condition mimicking ovarian malignancy that required surgical excision of the affected ovary.
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Abstract
Xanthogranulomatous oophoritis is a rare condition characterized by chronic inflammation and destruction of ovarian tissue. This case report describes a 25-year-old woman who presented with symptoms of bleeding, abdominal pain, and fever. Imaging revealed a tubo-ovarian mass, and during surgery, a pus-filled mass adhered to the right ovary was excised. Histopathological examination confirmed xanthogranulomatous oophoritis, and the pus culture showed the presence of coagulase- negative Staphylococcus aureus. This condition is often mistaken for ovarian malignancy and requires surgical removal of the affected ovary. Antibiotic therapy has not been successful in reducing the ovarian mass.
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Too few in-corpus citations on either side for a chart; here are the lists.
Cites (3)
- Xanthogranulomatous Oophoritis: An Unusual Complication of Typhoid 1995
- Xanthogranulomatous endometritis and oophoritis secondary to diverticulitis. A rare cause of postmenopausal bleeding 2007
- Xanthomatous oophoritis following uterine artery embolisation: successful conservative surgical management with favourable outcome 2013
References (11)
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