Structured Summary
Abstract
A nonproliferative disorder of PLASMA CELLS characterized by excessive production and misfolding of IMMUNOGLOBULIN LIGHT CHAINS that form insoluble amyloid fibrils (see AMYLOID DEPOSITS) in various tissues. Clinical features include LIVER FAILURE; MULTIPLE MYELOMA; NEPHROTIC SYNDROME; RESTRICTIVE CARDIOMYOPATHY, and neuropathies.
MeSH Record
Classification
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MeSH Record
Synonyms
17 entry terms
- AL Amyloidosis
- Amyloidosis, Immunoglobulin Light-chain
- Amyloidosis, Primary
- Monoclonal Immunoglobulin Deposition Disease
- Primary Amyloidosis
- Primary Systemic Amyloidosis
- AL Amyloidoses
- Amyloidoses, Primary
- Amyloidoses, Primary Systemic
- Amyloidosis, Immunoglobulin Light chain
- Amyloidosis, Primary Systemic
- Immunoglobulin Light chain Amyloidosis
- Immunoglobulin Light-chain Amyloidoses
- Primary Amyloidoses
- Primary Systemic Amyloidoses
- Systemic Amyloidoses, Primary
- Systemic Amyloidosis, Primary
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2018(2010)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Immunoglobulin Light-chain Amyloidosis. Medical Subject Headings (MeSH). 2026. Unique ID D000075363. http://id.nlm.nih.gov/mesh/2026/D000075363
- Immunoglobulin Light-chain Amyloidosis. In: Wikipedia. https://en.wikipedia.org/wiki/AL_amyloidosis
- Immunoglobulin Light-chain Amyloidosis. In: Wikidata. https://www.wikidata.org/wiki/Q4652470