Linder J, Silberman H R, Croker B P
Am J Clin Pathol. 1982 Dec;78(6):864-7. doi: 10.1093/ajcp/78.6.864.
A patient development renal failure following a ten-year affliction with hairy cell leukemia. Renal biopsy showed amyloidosis, characterized by the presence of potassium permagnate-sensitive congophilia in deposits within glomeruli and renal blood vessels. Electron microscopy demonstrated amyloid fibrils. Immunohistochemical technics showed the deposits were composed of AA Protein. These Congo red staining properties, and the presence of AA Protein are characteristic of deposits in secondary amyloidosis. Secondary amyloidosis is a known complication of many chronic illnesses. This report shows it may concur with hairy cell leukemia, and that amyloidosis should be considered in the differential diagnosis of renal failure in patients with hairy cell leukemia.
一名患毛细胞白血病十年的患者出现了肾衰竭。肾活检显示为淀粉样变性,其特征是在肾小球和肾血管内的沉积物中存在对高锰酸钾敏感的嗜刚果红性。电子显微镜显示有淀粉样纤维。免疫组织化学技术表明沉积物由AA蛋白组成。这些刚果红染色特性以及AA蛋白的存在是继发性淀粉样变性沉积物的特征。继发性淀粉样变性是许多慢性疾病的已知并发症。本报告表明它可能与毛细胞白血病同时发生,并且在毛细胞白血病患者肾衰竭的鉴别诊断中应考虑淀粉样变性。