Resumen de Manifestaciones cutáneas de amiloidosis sistémica como clave diagnóstica: Caso clínico
Felix Fich Schilcrot, Marco Chahuan, M.M. Farías, Consuelo Cárdenas D, Álvaro Abarzúa, Gabriela Araya, Sergio González B.
Background: Systemic amyloidosis is a rare disease that can affect any organ. Its clinical manifestations are varied and nonspecific. The skin involvement of this disease is common and can be easily recognized on physical examination. We report a 57-year-old male presenting with a two years history of malaise, dyspnea and myalgias. On physical examination, ungueal dystrophy, orange pigmentation of eyelids with periocular petechiae and mild macroglossia were observed. Incisional biopsies of the eyelids, cheeks and hands were obtained. The pathological study demonstrated amyloid deposits. Since protein electrophoresis was normal, the diagnosis of AA amyloidosis was postulated.
