Hidden amyloidosis in liver and bone marrow

Gayathri Jagadish, M. Archana, K. S. Nataraj, Sandeep Desai, Vishnu Kurpad
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Abstract

Primary amyloidosis and multiple myeloma (MM) involve clonal plasma cell proliferation. Approximately 10–15% of patients with amyloidosis have MM. Characteristic apple-green birefringence using Congo red staining on polarized microscopy confirms amyloid. MM is prevalent at ages from 60 to 70 years. Amyloidosis commonly affects the heart, kidneys, gastrointestinal tract/liver and peripheral or autonomic nervous system predicting a poor prognosis due to organ deterioration. This case highlights the importance of diagnosing amyloidosis in a 60-year-old female where plasma cells were present in the liver and bone marrow along with amyloid deposits and for early initiation of intense chemotherapy.
肝脏和骨髓中的隐性淀粉样变性
原发性淀粉样变性和多发性骨髓瘤(MM)涉及克隆性浆细胞增殖。约有 10-15% 的淀粉样变性患者患有多发性骨髓瘤。在偏光显微镜下使用刚果红染色法可确认淀粉样蛋白具有苹果绿双折射特征。淀粉样变性的发病年龄为 60 至 70 岁。淀粉样变性通常会影响心脏、肾脏、胃肠道/肝脏、外周或自主神经系统,由于器官退化,预后较差。本病例强调了对一名肝脏和骨髓中出现浆细胞和淀粉样蛋白沉积的 60 岁女性进行淀粉样变性诊断的重要性,以及及早启动强化疗的重要性。
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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