Immunoblastic Lymphadenopathy
"Immunoblastic Lymphadenopathy" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D007119
|
| MeSH Number(s) |
C15.604.338.500 C15.604.515.509 C20.683.515.501
|
| Concept/Terms |
Immunoblastic Lymphadenopathy- Immunoblastic Lymphadenopathy
- Angioimmunoblastic Lymphadenopathy
- Angioimmunoblastic Lymphadenopathies
- Lymphadenopathies, Angioimmunoblastic
- Lymphadenopathy, Angioimmunoblastic
- Lymphadenopathy, Immunoblastic
- Immunoblastic Lymphadenopathies
- Lymphadenopathies, Immunoblastic
|
Below are MeSH descriptors whose meaning is more general than "Immunoblastic Lymphadenopathy".
Below are MeSH descriptors whose meaning is more specific than "Immunoblastic Lymphadenopathy".
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Below are the most recent publications written about "Immunoblastic Lymphadenopathy" by people in Profiles.
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CD4-CD8- thymocytes from MRL-lpr/lpr mice exhibit abnormal proportions of alpha beta- and gamma delta-TCR+ cells and demonstrate defective responsiveness when activated through the TCR. Cell Immunol. 1991 Oct 15; 137(2):269-82.