Editorial
Copyright ©2011 Baishideng Publishing Group Co.
World J Gastrointest Endosc. Aug 16, 2011; 3(8): 157-161
Published online Aug 16, 2011. doi: 10.4253/wjge.v3.i8.157
Table 1 Comparison of characteristics of amyloid light chains and amyloid A amyloidosis[1,2,6,7]
amyloid light chains amyloidosisamyloid A amyloidosis
CausesIdiopathy and plasma cell dyscrasiasChronic inflammatory disorders and infections
DepositionMonoclonal immunoglobulin light chainsSerum amyloid A protein
Gastrointestinal site of amyloid depositionThe muscularis mucosae, submucosa and muscularis propriaThe propria mucosae
Gastrointestinal symptomsConstipation, mechanical obstruction and chronic intestinal pseudo-obstructionDiarrhea, malabsorption and weight loss
Endoscopic and radiological featuresPolypoid protrusions and thickening of the foldsFine granular appearance and mucosal friability
TreatmentsProkinetic agents and myeloma-type chemotherapyControl of the underlying inflammatory disorders