[Amyloidosis. A review]
- PMID: 10377850
[Amyloidosis. A review]
Abstract
Amyloidosis is a heterogenous group of diseases, all characterized by extracellular deposition of amyloid either systemically or localized. Of wellknown diseases are Alzheimer's dementia, AL-amyloidosis (e.g. in multiple myeloma) and AA-amyloidosis (e.g. in rheumatoid arthritis). Amyloid is composed of three components of which the fibrillary component is the basis of amyloid classification. Many types of amyloid have a systemic distribution and give rise to varying symptoms. The diagnosis is based on biopsy, preferably of abdominal subcutis. The prognosis is poor, however, recent investigations on the three-dimensional structure of the P-component provide hope for future therapy.
Similar articles
-
Diagnostic and therapeutic approach of systemic amyloidosis.Neth J Med. 2004 Apr;62(4):121-8. Neth J Med. 2004. PMID: 15255082 Review.
-
Renal amyloidosis in childhood. An overview of the topic with 25 years experience.Turk J Pediatr. 1995 Oct-Dec;37(4):357-73. Turk J Pediatr. 1995. PMID: 8560604 Review.
-
[Amyloidosis: definition and classification].Arch Anat Cytol Pathol. 1996;44(2-3):101-5. Arch Anat Cytol Pathol. 1996. PMID: 8794589 French.
-
[Interdisciplinary guidelines on diagnosis and treatment for extracerebral amyloidoses--published by the German Society of Amyloid Diseases (www.amyloid.de)].Dtsch Med Wochenschr. 2006 Jul 7;131(27 Suppl 2):S45-66. doi: 10.1055/s-2006-947836. Dtsch Med Wochenschr. 2006. PMID: 16835821 German.
-
[Interdisciplinary guidelines for diagnosis and therapy of extracerebral amyloidosis: issued by the German Society of Amyloid Diseases e. V. (www.amyloid.de)].Med Klin (Munich). 2006 Oct 15;101(10):825-9. doi: 10.1007/s00063-006-1110-0. Med Klin (Munich). 2006. PMID: 17039325 German. No abstract available.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical