Hashimoto M, Shingu M, Yoshikawa Y, Nonaka S, Wada T, Ichibanngase Y, Nobunaga M
Department of Clinical Immunology, Kyushu University, Beppu-city.
Ryumachi. 1995 Feb;35(1):100-6.
We herein report two cases of gastrointestinal amyloidosis, secondary to juvenile rheumatoid arthritis (JRA) in one, and rheumatoid arthritis (RA) in the other. A 21-year-old woman, who has been suffering from JRA for the past 12 years, was transferred to our hospital due to intense pain in the epigastrium and back, diarrhea, high fever, and paralytic ileus. Treatment by corticosteroid, antibiotics, protease inhibitor, and total parenteral nutrition was not effective. The laparoscopic surgery was performed because of repeated melena followed by an episode of hypovolemic shock. The resected specimen of the ileum showed histologically marked amyloid deposition in the arteriolar walls. A 83-year-old man with RA for 14 years, was admitted to our hospital with complaints of abdominal pain, nausea, and diarrhea. He underwent an emergency operation for perforation of the ileum. The resected specimen revealed amyloid deposition and non-caseating granulomas. The fragility and impaired blood supply caused by amyloid deposition in the vascular walls may have terminated in the severe intestinal lesion. Further clinicopathological studies along this line are keenly desired in order to establish therapeutic modalities for gastrointestinal amyloidosis.
我们在此报告两例胃肠道淀粉样变性病例,其中一例继发于青少年类风湿性关节炎(JRA),另一例继发于类风湿性关节炎(RA)。一名21岁女性,在过去12年中一直患有JRA,因上腹部和背部剧痛、腹泻、高热及麻痹性肠梗阻被转至我院。使用皮质类固醇、抗生素、蛋白酶抑制剂及全胃肠外营养治疗均无效。因反复黑便并随后出现一次低血容量性休克而进行了腹腔镜手术。切除的回肠标本在组织学上显示小动脉壁有明显的淀粉样沉积。一名83岁男性,患RA 14年,因腹痛、恶心和腹泻入院。他因回肠穿孔接受了急诊手术。切除的标本显示有淀粉样沉积和非干酪样肉芽肿。血管壁淀粉样沉积导致的脆弱性和血供受损可能最终引发了严重的肠道病变。迫切需要沿着这条线进行进一步的临床病理研究,以建立胃肠道淀粉样变性的治疗方法。