Marsh W M, Streeten B W, Hoepner J A, Zhang W, Davey F R
Ophthalmology. 1987 Jan;94(1):61-4. doi: 10.1016/s0161-6420(87)33508-0.
A 62-year-old man was found to have a large asymptomatic amyloid nodule of the conjunctiva. Within the next year, a diffuse mixed small and large cell lymphoma of his scapula developed with amyloid in its stroma. No abnormal serum or urine protein was found. Subsequently, rib and paraspinal masses appeared. After irradiation and chemotherapy, the patient died of bronchopneumonia, 3 years after onset. By immunostaining, the amyloid of both conjunctiva and scapular tumor was of polyclonal immunoglobulin (AL) type, most prominently IgG and lambda chains, with lesser staining for IgA and kappa chains. The tumor cells showed a similar pattern. To our knowledge, this is the first report of systemic lymphoma and localized conjunctival amyloidosis without a serum paraprotein, and the first such association with a lymphoma of this cell type. Immunotyping of conjunctival amyloidosis should be performed to guide the workup for possible systemic disease.
一名62岁男性被发现患有一个大的无症状结膜淀粉样瘤。在接下来的一年里,他的肩胛骨出现了弥漫性混合小细胞和大细胞淋巴瘤,其基质中有淀粉样物质。未发现血清或尿液蛋白异常。随后,肋骨和椎旁出现肿块。放疗和化疗后,患者在发病3年后死于支气管肺炎。通过免疫染色,结膜和肩胛部肿瘤的淀粉样物质均为多克隆免疫球蛋白(AL)型,最显著的是IgG和λ链,IgA和κ链染色较少。肿瘤细胞显示出类似的模式。据我们所知,这是首例无血清副蛋白的系统性淋巴瘤和局限性结膜淀粉样变性的报告,也是首例这种细胞类型淋巴瘤的此类关联。应进行结膜淀粉样变性的免疫分型,以指导对可能的系统性疾病的检查。