Cutaneous manifestations in three patients with systemic amyloidosis

Main Article Content

Natalia Mendoza Plata
Ana Cristina Ruiz
Luis Fernando Pinto
Luz Adriana Vásquez Ochoa
María Isabel Arredondo Ossa

Abstract

Systemic amyloidosis is a group of heterogeneous diseases caused by tissue deposition of misfolded proteins. We report 3 cases of patients with systemic amyloidosis. Diagnosis in all cases was confirmed by biopsy. Here, we also briefly review the pathogenesis, diagnosis, treatment, and clinical manifestations, with a particular focus on cutaneous manifestations. Since such lesions appear early in the disease, we consider that accurately identifying them can have an impact on the prognosis of this affection.


 


 


 

Keywords:
amyloidosis, purpura, macroglossia

Article Details

Author Biographies

Natalia Mendoza Plata, Pontifical Bolivarian University

Dermatology Resident, Universidad Pontificia Bolivariana. Medellin Colombia.

Ana Cristina Ruiz, Hospital Pablo Tobon Uribe

Dermatopathologist, Hospital Pablo Tobón Uribe. Medellin Colombia.

Luis Fernando Pinto, Hospital Pablo Tobon Uribe

Rheumatologist, Pablo Tobón Uribe Hospital. Medellin Colombia

Luz Adriana Vásquez Ochoa, Hospital Pablo Tobon Uribe

Dermatologist, Pablo Tobón Uribe Hospital. Medellin Colombia

María Isabel Arredondo Ossa, Hospital Pablo Tobon Uribe

Dermatologist, Pablo Tobón Uribe Hospital. Medellin Colombia

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