血管瘤样纤维组织细胞瘤1例并文献复习

Q4 Medicine
Gerardo Cazzato, A. Colagrande, A. Cimmino, Mariella Silecchia, T. Lettini, L. Resta, G. Ingravallo
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引用次数: 1

摘要

血管瘤样纤维组织细胞瘤是一种罕见的具有中等恶性潜能的肿瘤,主要发生在皮下,以结节状和合胞生长模式的不同比例的上皮样细胞、卵形细胞和梭形细胞为特征,并伴有出血性假血管间隙。在这里,我们报告了一个68岁男性的临床病例,他表现为右臂AFH;这种疾病在手术切除几年后复发。我们还对文献进行了简要的回顾,重点是生物学和遗传特征以及与其他或多或少相似实体的鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Angiomatoid Fibrous Histiocytoma: Case Presentation with Review of Literature
Angiomatoid fibrous histiocytoma is a rare neoplasm with an intermediate malignant potential, that mostly occurs in the subcutis and features varying proportions of epithelioid, ovoid and spindle cells in a nodular and syncytial growth pattern, with hemorrhagic pseudovascular spaces. Here, we report the clinical case of a 68-year-old man who presented with AFH on the right arm; the disease relapsed a few years after surgical excision. We also conduct a brief review of the literature, focusing on the biological and genetic characteristics and the differential diagnosis from other more or less similar entities.
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来源期刊
Clinical Osteology
Clinical Osteology Medicine-Endocrinology, Diabetes and Metabolism
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