AA amyloidosis is a complication of chronic diseases associated with the activation of acute phase reactants. The precursor of amyloid is the serum amyloid A. The kidneys are the most frequently involved, but amyloid can be deposited in any internal organ. AA amyloidosis often develops after many years of chronic illness, but its occurrence is a poor prognostic factor. Untreated leads to renal failure. For diagnosis of AA amyloidosis, histopathological confirmation is necessary. Staining with Congo red is a standard diagnostic test. Aspiration of abdominal fat is the preferred way to obtain the material for diagnostic testing. Normalization of inflammatory parameters and, as a consequence, the lack of the precursor of the deposited amyloid ...
Kidney amyloid deposition is one of the most common and most severe manifestations of systemic amylo...
Antiphospholipid syndrome (APS) is an autoimmune systemic disease characterized by recurrent venous ...
Primary systemic light-chain amyloidosis (AL) that accounts for 4/5 of all cases can be manifested a...
Light chain amyloidosis (AL amyloidosis) is a disease in which monoclonal immunoglobulin light chain...
Amyloidozy to heterogenna grupa chorób, której istotą jest odkładanie się nierozpuszczalnych włókien...
Amyloidosis AA (reactive amyloidosis) is a result of long-lasting inflammatory process. Nowadays, in...
Amyloidosis is a heterogeneous group of diseases in which symptoms develop due to deposition of amyl...
Amyloidozy to heterogenna grupa chorób, których istotą jest odkładanie się nierozpuszczalnych włókie...
The leading strategy in the management of systemic amyloidosis is currently focused on reducing the...
Light chain amyloidosis (AL amyloidosis) is a systemic disease leading to organ damage due to deposi...
The systemic amyloidosis are diseases induced by misfolded proteins. These insoluble proteins deposi...
Light-chain amyloidosis (amyloidosis AL) is diagnosed in approx. 70% of patients with cardiac amyloi...
We present a 69-year-old patient, in whom in March 2016 a monoclonal gammopathy of undeterminedsigni...
Treatment of patients with light chain amyloidosis (AL amyloidosis) is a challenge in routine clinic...
Antiphospholipid syndrome (APS) was described by Hughes et al in 1986 and then by Harris et al in 19...
Kidney amyloid deposition is one of the most common and most severe manifestations of systemic amylo...
Antiphospholipid syndrome (APS) is an autoimmune systemic disease characterized by recurrent venous ...
Primary systemic light-chain amyloidosis (AL) that accounts for 4/5 of all cases can be manifested a...
Light chain amyloidosis (AL amyloidosis) is a disease in which monoclonal immunoglobulin light chain...
Amyloidozy to heterogenna grupa chorób, której istotą jest odkładanie się nierozpuszczalnych włókien...
Amyloidosis AA (reactive amyloidosis) is a result of long-lasting inflammatory process. Nowadays, in...
Amyloidosis is a heterogeneous group of diseases in which symptoms develop due to deposition of amyl...
Amyloidozy to heterogenna grupa chorób, których istotą jest odkładanie się nierozpuszczalnych włókie...
The leading strategy in the management of systemic amyloidosis is currently focused on reducing the...
Light chain amyloidosis (AL amyloidosis) is a systemic disease leading to organ damage due to deposi...
The systemic amyloidosis are diseases induced by misfolded proteins. These insoluble proteins deposi...
Light-chain amyloidosis (amyloidosis AL) is diagnosed in approx. 70% of patients with cardiac amyloi...
We present a 69-year-old patient, in whom in March 2016 a monoclonal gammopathy of undeterminedsigni...
Treatment of patients with light chain amyloidosis (AL amyloidosis) is a challenge in routine clinic...
Antiphospholipid syndrome (APS) was described by Hughes et al in 1986 and then by Harris et al in 19...
Kidney amyloid deposition is one of the most common and most severe manifestations of systemic amylo...
Antiphospholipid syndrome (APS) is an autoimmune systemic disease characterized by recurrent venous ...
Primary systemic light-chain amyloidosis (AL) that accounts for 4/5 of all cases can be manifested a...