Structured Summary
Abstract
A disorder characterized by proliferation of arborizing small vessels, prominent immunoblastic proliferations and amorphous acidophilic interstitial material. Clinical manifestations include fever, sweats, weight loss, generalized lymphadenopathy and frequently hepatosplenomegaly.
MeSH Record
Classification
Broader headings
Related Concepts
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MeSH Record
Synonyms
7 entry terms
- Angioimmunoblastic Lymphadenopathy
- Lymphadenopathy, Immunoblastic
- Angioimmunoblastic Lymphadenopathies
- Immunoblastic Lymphadenopathies
- Lymphadenopathies, Angioimmunoblastic
- Lymphadenopathies, Immunoblastic
- Lymphadenopathy, Angioimmunoblastic
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
79
MeSH Hierarchy
Tree Numbers
MeSH Record
NLM Classification
WH 720
AMA Style
References
- National Library of Medicine. Immunoblastic Lymphadenopathy. Medical Subject Headings (MeSH). 2026. Unique ID D007119. http://id.nlm.nih.gov/mesh/2026/D007119
- Immunoblastic Lymphadenopathy. In: Wikidata. https://www.wikidata.org/wiki/Q55093037