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首页> 外文期刊>Gynecologic Oncology: An International Journal >Primary giant cell malignant fibrous histiocytoma of the ovary: case report and review of the literature.
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Primary giant cell malignant fibrous histiocytoma of the ovary: case report and review of the literature.

机译:卵巢原发性巨细胞恶性纤维组织细胞瘤:病例报告及文献复习。

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摘要

Primary sarcomas represent 2-3% of all female genital tract malignancies; only 10% of these are extra-uterine [1]. Malignant fibrous histiocytoma (MFH) arises from primitive mesenchymal cells and is the most common sarcoma of late adult life [2]. Under the World Health Organization re-classification (2002), four subtypes exist with varying prevalence: storiform/pleomorphic MFH (undifferentiated high-grade pleomorphic sarcoma, 60%), myxoid MFH (myofibrosarcoma, 25%), giant cell MFH (undifferentiated pleomorphic sarcoma with giant cells, 10%), and inflammatory MFH (undifferentiated pleomorphic sarcoma with prominent inflammation, 5%) [3]. Only 5 cases of primary MFH of the ovary have been reported and encompass the inflammatory, pleomorphic, and myxoid variants (Table 1). We now describe the first instance of giant cell MFH arising from the ovary.
机译:原发性肉瘤占所有女性生殖道恶性肿瘤的2-3%;其中只有10%是子宫外的[1]。恶性纤维组织细胞瘤(MFH)起源于原始间充质细胞,是成年晚期最常见的肉瘤[2]。根据世界卫生组织的重新分类(2002),存在四种亚型,其患病率各不相同:星形/多形性MFH(未分化的高级多形性肉瘤,60%),粘液性MFH(肌原纤维肉瘤,25%),巨细胞MFH(未分化的多形性)具有巨细胞的肉瘤,占10%)和发炎的MFH(具有明显炎症的未分化多形性肉瘤,占5%)[3]。仅报道了5例卵巢原发性MFH,包括炎症性,多形性和粘液样变体(表1)。现在我们描述由卵巢产生的巨细胞MFH的第一个实例。

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