A Study on Plasmacytoma

Satish Deshmukh, Sushrut M. Fulare, Shriniket Sawarkar
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Abstract

Plasmacytoma a neoplastic proliferation of plasma cells is one of the forms of plasma cell dyscrasia that may manifest as multiple myeloma, primary amyloidosis, or monoclonal gammopathy of unknown significance. Factors such as viral pathogenesis and irritation from inhaled irritants have been noted. Genetic factors may also play a role; however, no specific loci for the origin of this disease have been identified. Plasmacytoma mainly affects people in the 5th to 6th decade of their lives. Diagnostic criteria for SP (published by the International Myeloma Working Group, IMWG) indicate that the lesion must be solitary in nature without clinical, radiographical or biochemical evidence of systemic MM. Recent guidelines recommend MRI or PET/CT evaluation, in addition to standard x-ray skeletal survey, to exclude multifocal disease [1].
浆细胞瘤的研究
浆细胞瘤是浆细胞增生的肿瘤,是浆细胞病变的一种形式,可表现为多发性骨髓瘤、原发性淀粉样变性或意义不明的单克隆伽玛病。病毒致病机制和吸入刺激物的刺激等因素已被注意到。遗传因素也可能起作用;然而,没有确定这种疾病起源的特定位点。浆细胞瘤主要影响5 - 6岁的人。SP的诊断标准(由国际骨髓瘤工作组(IMWG)发布)表明,病变必须是孤立性的,没有系统性MM的临床、影像学或生化证据。最近的指南建议,除了标准的x线骨骼检查外,还应进行MRI或PET/CT评估,以排除多灶性疾病[1]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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