Kuroha Masatake, Yoshinaga Tsuneaki, Yazaki Masahide, Fujishima Fumiyoshi, Handa Tomoyuki, Suzuki Kaoru, Hishinuma Kasumi, Masu Yutaro, Shimoyama Yusuke, Naito Takeo, Moroi Rintaro, Kanazawa Yoshitake, Shiga Hisashi, Kakuta Yoichi, Masamune Atsushi
Division of Gastroenterology, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, 980-8574, Japan.
Shinshu University, Institute for Biomedical Sciences, Matsumoto, Japan.
Clin J Gastroenterol. 2021 Jun;14(3):815-819. doi: 10.1007/s12328-021-01378-7. Epub 2021 Apr 26.
Amyloidosis is classifiable as systemic, with amyloid deposition in organs throughout the body, or localized, involving only one organ. Amyloidosis localized in the intestinal tract is rare. This report describes three cases of localized AL amyloidosis in the intestinal tract and presents their clinical characteristics, endoscopic findings, and prognoses. All three cases were asymptomatic, and were found accidentally during endoscopy for closer examination after a positive fecal occult blood test. Endoscopic findings included patchy redness and meandering dilated vessels of the lesion. Using autofluorescence (AFI) endoscopy, the lesion of amyloid deposition was enhanced as bright green. We used fluorescence microscopy to observe unstained specimens obtained from an amyloid deposition site with excitation light. Autofluorescence was detected with the broad excitation wavelength at amyloid deposition lesion sites of the specimen. Results revealed that AL amyloid has autofluorescence that engenders its detection by AFI endoscopy as bright green. In none of the three cases was systemic amyloidosis or organ failure observed. The long-term course of all the cases was favorable.
淀粉样变性可分为全身性,即淀粉样蛋白沉积于全身各器官,或局限性,仅累及一个器官。局限于肠道的淀粉样变性很少见。本报告描述了3例肠道局限性AL淀粉样变性病例,并介绍了其临床特征、内镜检查结果及预后。所有3例均无症状,均在粪便潜血试验阳性后因进一步检查而在内镜检查时偶然发现。内镜检查结果包括病变部位散在发红和迂曲扩张的血管。使用自体荧光(AFI)内镜检查时,淀粉样蛋白沉积病变呈亮绿色增强。我们使用荧光显微镜观察从淀粉样蛋白沉积部位获取的未染色标本,并使用激发光进行观察。在标本的淀粉样蛋白沉积病变部位,用宽激发波长检测到自体荧光。结果显示,AL淀粉样蛋白具有自体荧光,通过AFI内镜检查可将其检测为亮绿色。3例均未观察到全身性淀粉样变性或器官衰竭。所有病例的长期病程良好。