Lee D D, Huang C Y, Wong C K, Kao K P
Department of Dermatology, National Yang-Ming University, Taipei, Taiwan, Republic of China.
J Dermatol. 1996 Apr;23(4):296-8. doi: 10.1111/j.1346-8138.1996.tb04018.x.
We report a case of systemic amyloidosis with the initial sign of polyneuropathy. The patient eventually developed heart failure, macroglossia, and ecchymoses 6 years later. Biopsies from the sural nerve and normal-looking skin both proved the existence of amyloid.
我们报告一例以多发性神经病为初始症状的系统性淀粉样变性病例。6年后,该患者最终出现心力衰竭、巨舌和瘀斑。腓肠神经活检以及外观正常的皮肤活检均证实存在淀粉样物质。