What is amyloidosis PPT?

◎Definition : Amyloid refers to an abnormal deposit of insoluble polymeric protein fibrils in tissues and organs. This condition of deposition of amyloid in tissues is known as Amyloidosis. 5. • The fibrils are formed by the aggregation of misfolded, normally soluble proteins .

What is systemic amyloid?

Secondary systemic amyloidosis is a disorder in which abnormal proteins build up in tissues and organs. Clumps of the abnormal proteins are called amyloid deposits. Secondary means it occurs because of another disease or situation.

What is primary systemic amyloidosis?

Primary systemic amyloidosis involves the deposition of insoluble monoclonal immunoglobulin (Ig) light (L) chains or L-chain fragments in various tissues, including smooth and striated muscles, connective tissues, blood vessel walls, and peripheral nerves.

What is the meaning of amyloidosis?

Amyloidosis is the name for a group of rare, serious conditions caused by a build-up of an abnormal protein called amyloid in organs and tissues throughout the body. The build-up of amyloid proteins (deposits) can make it difficult for the organs and tissues to work properly.

What is the diagnosis of primary systemic amyloidosis?

Primary systemic amyloidosis is referred to as AL amyloidosis, with the A signifying amyloid and the L designating it as light-chain amyloidosis. Terms such as AL describe the protein (light chain), but do not necessarily describe the clinical phenotype.

Which is the best PPT presentation for amyloidosis?

Autopsy Photo Histopathology Autopsy Findings Amyloid Pathogenesis Classification Types of Amyloidosis Types of Amyloidosis Type of Amyloidosis Major | PowerPoint PPT presentation | free to view Recognizing the Patient with AA Amyloidosis: Factors Critical to Diagnosis – Referral from many surgical pathologists throughout Germany and Europe

What are the different types of amyloidosis proteins?

CLASSIFICATION OF AMYLOIDOSIS (AL= Amyloid light chain; AA= Amyloid-associated protein; Aβ2M= Amyloid β2- microglobulin; ATTR= Amyloid transthyretin; APrP=Amyloid of prion proteins, Aβ= β- amyloid protein). www.facebook.com/notesdental 10.

Where does amyloidosis occur in the human body?

Primary systemic amyloidosis involves the deposition of insoluble monoclonal immunoglobulin (Ig) light (L) chains or L-chain fragments in various tissues, including smooth and striated muscles, connective tissues, blood vessel walls, and peripheral nerves. [ 1]