Systemic amyloidosis is a rare disease that can affect any organ. Its clinical manifestations are varied and nonspecifi c. 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
AbstractSystemic amyloidosis is a rare disease that can be rapidly progressive due to widespread org...
Background: Amyloidosis is characterized by the extracellular deposit of an insoluble fibrillar prot...
Systemic immunoglobulin light chain amyloidosis is the most common and severe type of amyloidosis. T...
A 61-year-old man presented for evaluation of a bruise-like lesion of the right knee. He was found t...
Primary Systemic Amyloidosis (AL) is the most frequent form of systemic amyloidosis and its morbilil...
Primary Systemic Amyloidosis (AL) is the most frequent form of systemic amyloidosis and its morbilil...
Primary systemic amyloidosis is a rare disease. It primarily involves kidney, heart, peripheral nerv...
Abstract: Systemic light chain amiloydosis is a rare disease. Due to its typical cutaneous lesions, ...
A 65-year-old male presented with hemorrhagic bullous skin lesions with purpura and ecchymoses. Ther...
Primary localized cutaneous amyloidosis refers to a group of disorders characterized by deposition o...
Amyloidosis is part of a group of deposition diseases. Nodular amyloidosis is a rare form of primary...
open14noFunding was provided by Associazione Italiana per la Ricerca sul Cancro.Muscle involvement i...
Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Li...
The patient was a 56-year-old female. The whole body has brown patches for 16 years. Dermatological ...
This case report is about a 48-year-old female patient with systemic amyloidosis and multiple myelom...
AbstractSystemic amyloidosis is a rare disease that can be rapidly progressive due to widespread org...
Background: Amyloidosis is characterized by the extracellular deposit of an insoluble fibrillar prot...
Systemic immunoglobulin light chain amyloidosis is the most common and severe type of amyloidosis. T...
A 61-year-old man presented for evaluation of a bruise-like lesion of the right knee. He was found t...
Primary Systemic Amyloidosis (AL) is the most frequent form of systemic amyloidosis and its morbilil...
Primary Systemic Amyloidosis (AL) is the most frequent form of systemic amyloidosis and its morbilil...
Primary systemic amyloidosis is a rare disease. It primarily involves kidney, heart, peripheral nerv...
Abstract: Systemic light chain amiloydosis is a rare disease. Due to its typical cutaneous lesions, ...
A 65-year-old male presented with hemorrhagic bullous skin lesions with purpura and ecchymoses. Ther...
Primary localized cutaneous amyloidosis refers to a group of disorders characterized by deposition o...
Amyloidosis is part of a group of deposition diseases. Nodular amyloidosis is a rare form of primary...
open14noFunding was provided by Associazione Italiana per la Ricerca sul Cancro.Muscle involvement i...
Trabalho Final do Curso de Mestrado Integrado em Medicina, Faculdade de Medicina, Universidade de Li...
The patient was a 56-year-old female. The whole body has brown patches for 16 years. Dermatological ...
This case report is about a 48-year-old female patient with systemic amyloidosis and multiple myelom...
AbstractSystemic amyloidosis is a rare disease that can be rapidly progressive due to widespread org...
Background: Amyloidosis is characterized by the extracellular deposit of an insoluble fibrillar prot...
Systemic immunoglobulin light chain amyloidosis is the most common and severe type of amyloidosis. T...