Iwai M, Ishii Y, Mori T, Harada Y, Kitagawa Y, Kashiwadani M, Ou O, Okanoue T, Kashima K
Third Department of Internal Medicine, Kyoto Prefectural University of Medicine, Japan.
J Clin Gastroenterol. 1999 Mar;28(2):162-6. doi: 10.1097/00004836-199903000-00017.
Two patients with primary amyloidosis (amyloid light chain case) and severe cholestatic jaundice are described. Liver biopsy in the preterminal stage demonstrated amyloid deposits in the perisinusoidal space and in portal tracts, and hepatocytes were atrophic because of compression by amyloid fibrils. Ultrastructural findings showed amyloid fibrils not only in Disse's space but also in the sinusoids, and the hepatocyte microvilli facing the amyloid fibrils were spicular. There were aggregates of lysosomal granules in the vicinity of bile canaliculi and some bile canaliculi were dilated with loss of microvilli. Amyloid fibrils in the portal tract compressed bile ductules, causing wide intercellular space and separated basement membranes from their epitheliums. These findings suggested disturbance in transporting not only of essential materials from sinusoids to hepatocytes but also of secretory vesicles into bile canaliculi and leakage of bile juice from small bile ductules in preterminal stage of primary amyloidosis.
本文描述了两名原发性淀粉样变性患者(轻链型淀粉样变病例),他们均伴有严重的胆汁淤积性黄疸。临终前期的肝活检显示,窦周间隙和门管区存在淀粉样蛋白沉积,肝细胞因受淀粉样纤维压迫而萎缩。超微结构研究结果表明,狄氏间隙和肝血窦内均有淀粉样纤维,肝细胞面向淀粉样纤维的微绒毛呈针状。胆小管附近有溶酶体颗粒聚集,部分胆小管扩张,微绒毛缺失。门管区内的淀粉样纤维压迫胆小管,导致细胞间隙增宽,基底膜与其上皮分离。这些结果提示,在原发性淀粉样变性临终前期,不仅存在从肝血窦到肝细胞的必需物质转运障碍,还存在分泌小泡向胆小管的转运障碍以及小胆管胆汁渗漏。