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AL amyloidosis is caused by the deposition of abnormal antibody free light chains. The abnormal light chains are produced by monoclonal plasma cells, and, although AL amyloidosis can occur without diagnosis of another disorder, it is often associated with other plasma cell disorders, such as multiple myeloma and Waldenström's macroglobulinemia. [6]
AL amyloidosis occurs in about 3–13 per million people per year and AA amyloidosis in about two per million people per year. [2] The usual age of onset of these two types is 55 to 60 years old. [2] Without treatment, life expectancy is between six months and four years. [2]
Prognosis: Life expectancy up to 30 years after symptom development: PrP systemic amyloidosis is an extremely rare and unusual form of inherited prion disease. Unlike ...
AA amyloidosis is a form of amyloidosis, a disease characterized by the abnormal deposition of fibers of insoluble protein in the extracellular space of various tissues and organs. In AA amyloidosis, the deposited protein is serum amyloid A protein (SAA), an acute-phase protein which is normally soluble and whose plasma concentration is highest ...
Wild-type transthyretin amyloid (WTTA), also known as senile systemic amyloidosis (SSA), [1] is a disease that typically affects the heart and tendons of elderly people. It is caused by the accumulation of a wild-type (that is to say a normal ) protein called transthyretin .
Based on symptoms and blood tests, confirmed by biopsy of the temporal artery [4] Differential diagnosis: Takayasu arteritis, [5] stroke, primary amyloidosis [6] Treatment: Steroids, bisphosphonates, proton-pump inhibitor [4] Prognosis: Life expectancy (typically normal) [4] Frequency ~ 1 in 15,000 people a year (> 50 years old) [2]
Primary cutaneous amyloidosis is a form of amyloidosis associated with oncostatin M receptor. [ 2 ] [ 3 ] This type of amyloidosis has been divided into the following types: [ 4 ] : 520 Macular amyloidosis is a cutaneous condition characterized by itchy, brown, rippled macules usually located on the interscapular region of the back.
LECT2 Amyloidosis (ALECT2) is a form of amyloidosis caused by the LECT2 protein. It was found to be the third most common (~3% of total) cause of amyloidosis in a set of more than 4,000 individuals studied at the Mayo Clinic; the first and second most common forms the disorder were AL amyloidosis and AA amyloidosis, respectively.
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