Xanthogranulomatous Oophoritis Mimicking an Ovarian Neoplasm: A Rare Case Report

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Xanthogranulomatous Oophoritis Mimicking an Ovarian Neoplasm: A Rare Case Report

Xanthogranulomatous inflammation of female genital tract is uncommon and is usually seen in endometrium. Only a few cases involving the ovary have been reported. Its clinical manifestations, imaging modalities, and gross features can mimic ovarian malignancy. Thus, a preoperative diagnosis of this entity is important to avoid radical surgical treatment. We report a case of xanthogranulomatous o...

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Xanthogranulomatous Oophoritis: A Rare Case Report

Background and Objective: Xanthogranulomatous oophritis is an uncommon, non-neoplastic, chronic process in which the affected organ is destroyed by massive cellular infiltration of foamy histiocytes admixed with multinucleated giant cells, plasma cells, fibroblasts, neutrophils, and foci of necrosis. The etiology of this entity is unknown, but it shares histopathological findin...

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Case Of Xanthogranulomatous Oophoritis.

Xanthogranulomatous inflammation is characterized by destruction of the tissues of the organ involved and replacement by chronic inflammatory cells such as lymphocytes, plasma cells, occasional neutrophils with or without multinucleated or Touton giant cells. Exact aetiology is not known but the theory of infection with organisms like Proteus, E coli, and Bacteroides fragilis is most popular. X...

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Sclerosing Stromal Tumor: A Rare Ovarian Neoplasm

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A case report of xanthogranulomatous osteomyelitis of the distal ulna mimicking a malignant neoplasm

PATIENT Male, 59 FINAL DIAGNOSIS: Xanthogranulomatous osteomyelitis Symptoms: Painful swelling in the wrist Medication: Drug history of antifulgal agents Clinical Procedure: Excisional biopsy Specialty: Radiology. OBJECTIVE Rare disease. BACKGROUND Xanthogranulomatous inflammation is a chronic inflammatory disease in which bone involvement is extremely rare. Bone involvement of xanthogranul...

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ژورنال

عنوان ژورنال: Journal of Mid-life Health

سال: 2018

ISSN: 0976-7800

DOI: 10.4103/jmh.jmh_111_17