Haraguchi H, Ohashi K, Yamada M, Hasegawa M, Maeda S, Komatsuzaki A
Department of Otorhinolaryngology, Tokyo Medical and Dental University, Japan.
ORL J Otorhinolaryngol Relat Spec. 1997 Jan-Feb;59(1):60-3. doi: 10.1159/000276907.
We describe a case of primary localized nodular tongue amyloidosis associated with Sjögren's syndrome in a 62-year-old woman. The presence of Sjögren's syndrome was confirmed both serologically and histologically. The amyloid tumor, which was marginally excised, recurred 3 years later and was re-excised. Immunohistochemical examination revealed that the amyloid protein was of the AL (lambda-light chain) type. Infiltration of plasma cells was observed around the minor salivary glands of the tongue surrounded by amyloid. The relationship between the plasma cells and amyloid deposition is discussed.
我们描述了一例62岁女性原发性局限性结节性舌淀粉样变性伴干燥综合征的病例。通过血清学和组织学检查证实了干燥综合征的存在。对淀粉样瘤进行了边缘切除,3年后复发并再次切除。免疫组化检查显示淀粉样蛋白为AL(λ轻链)型。在淀粉样物质包绕的舌小涎腺周围观察到浆细胞浸润。本文讨论了浆细胞与淀粉样物质沉积之间的关系。