额右浆细胞肉芽肿;病例报告

Daniel Rocandio-Hernández, Daniel Ballesteros-Herrera, M. Tena-Suck, Carlos Peñafiel-Salgado, Laura G. Chávez Macías, Erick Gmez Apo
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引用次数: 0

摘要

浆细胞肉芽肿是一种比较少见的病变,形成结节或团块,它是由多克隆浆细胞在故事状背景下纤维化和梭状细胞扩散而成。我们提出的情况下,62岁的妇女,有卵巢切除术的历史和增加体积在头部的右额区,然后呈现额叶综合征的神经学症状。影像学显示右侧额叶广泛性肿瘤扩散。组织学上肿瘤由浆细胞、B淋巴细胞浸润和大量血管组成。CD20、kappa、lambda、CD3、CD4均呈阳性。尽管它不常见,但它可以在任何地方发生,必须列入浆细胞瘤的鉴别诊断清单。轻链kappa和lambda的阳性表明了多克隆性,证实了诊断。
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Frontal Right Plasma Cell Granuloma; Case Report
The Plasma Cells Granuloma is a relatively rare lesion, that forms a nodule or a mass, it is conformed of polyclonal plasmatic cells in storiform background fibrosis and spread of fusiform cells. We present the case of a 62-year-old woman, with a history of oophorectomy and increased volume in the right frontal area of the head, then presenting neurologic signs of frontal lobe syndrome. Radiologic images showed a wide right frontal lobe neoplasia that spreads diffusely. Histologically the tumor was formed by plasma cells, B lymphocytes infiltrate, and numerous blood vessels. It was positive for CD20, kappa, lambda, CD3, and CD4. Even though it is uncommon, it can develop at any place and must be included in the differential diagnoses list for plasma cells neoplasia. The positivity of light chains kappa and lambda make evident the polyclonality that confirms the diagnosis.
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