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首页> 外文期刊>Journal of Clinical and Diagnostic Research >Endometrial Osseous Metaplasia?A Rare Presentation of Polymenorrhagia: A Case Report
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Endometrial Osseous Metaplasia?A Rare Presentation of Polymenorrhagia: A Case Report

机译:子宫内膜骨化生?多月经多发的罕见表现:一例报告

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Endometrial ossification is a rare entity in which bones are found in the uterus. Exact aetiopathogenesis is not known but the most accepted theory is metaplasia of stromal cells into osteoblast cells result in the formation of bones. The possibility of malignant mixed mullerian tumour should be in the mind of clinician and pathologist while making diagnosis. We hereby report an extremely rare case, which is among very few reported cases in the world, in which endometrial ossification presented in a perimenopausal female with polymenorrhagia. A 41-year-old multiparous patient presented with irregular bleeding per vaginum for the past two years. She was found to be a case of endometrial calcification with osseous metaplasia with presence of bones varying from 7mm ? 1.5 cms size in the uterine cavity. She was successfully managed by total abdominal hysterectomy.
机译:子宫内膜骨化是在子宫中发现骨骼的罕见实体。确切的发病机理尚不清楚,但最普遍接受的理论是基质细胞向成骨细胞的化生导致骨骼形成。进行诊断时,临床医生和病理学家应考虑恶性混合苗勒氏瘤的可能性。在此,我们报道了一种极罕见的病例,这是世界上极少数报道的病例,其中子宫内膜骨化是由绝经后女性多月经过多引起的。过去两年中,一名41岁的多产患者每阴道出现不规则出血。发现她是一例子宫内膜钙化伴骨化生,骨头直径在7mm?子宫腔内1.5 cms。她通过全腹子宫切除术成功进行了治疗。

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