Pashkova V S, Filippova L A
Arkh Patol. 1992;54(9):44-5.
It is a report of a rare case of amyloidosis in myeloma with a predominant localization in the caecum wall with the narrowing of blood vessels and a caecum gangrene and peritonitis as complications. Rarity of the case resulted in an erroneous clinical diagnosis and unjustified appendectomy.
这是一篇关于骨髓瘤合并淀粉样变性的罕见病例报告，主要病变位于盲肠壁，伴有血管狭窄，并引发盲肠坏疽和腹膜炎等并发症。该病例的罕见性导致了临床诊断错误和不必要的阑尾切除术。
