Yamada M, Hatakeyama S, Tsukagoshi H
Hum Pathol. 1985 Dec;16(12):1206-11. doi: 10.1016/s0046-8177(85)80032-0.
Gastrointestinal amyloid deposition was investigated in 21 autopsy cases of nonhereditary systemic amyloidosis, 18 of the AL (primary or myeloma-associated) type and three of the AA (secondary) type. Vascular deposition of amyloid, most apparent in the submucosa, was found in all cases. Parenchymal deposition was observed mainly in the muscularis mucosae and muscularis externa in the AL type, and in the lamina propria mucosae in the AA type. Comparison of amyloid deposition in the stomach and rectum revealed no differences for the AA type. In the AL type, however, deposition in the lamina propria mucosae and muscularis mucosae was more frequent and marked in the wall of the stomach than in the rectum. Thus, gastric biopsy would be more valuable than rectal biopsy in the diagnosis of AL amyloidosis.
对21例非遗传性系统性淀粉样变性尸检病例的胃肠道淀粉样沉积进行了研究,其中18例为AL(原发性或骨髓瘤相关性)型,3例为AA(继发性)型。所有病例均发现淀粉样物质在血管沉积,最明显的是在黏膜下层。实质性沉积在AL型主要见于黏膜肌层和外肌层,在AA型主要见于黏膜固有层。胃和直肠淀粉样沉积的比较显示,AA型无差异。然而,在AL型中,胃壁黏膜固有层和黏膜肌层的沉积比直肠更频繁且更明显。因此,在诊断AL型淀粉样变性时,胃活检比直肠活检更有价值。