| Descriptor English: | Immunoblastic Lymphadenopathy | ||||||
| Descriptor Spanish: |
Linfadenopatía Inmunoblástica
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| Descriptor Portuguese: | Linfadenopatia Imunoblástica | ||||||
| Descriptor French: | Lymphadénopathie angio-immunoblastique | ||||||
| Entry term(s): |
Angioimmunoblastic Lymphadenopathies Angioimmunoblastic Lymphadenopathy Immunoblastic Lymphadenopathies Lymphadenopathies, Angioimmunoblastic Lymphadenopathies, Immunoblastic Lymphadenopathy, Angioimmunoblastic Lymphadenopathy, Immunoblastic |
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| Tree number(s): |
C15.604.338.500 C15.604.515.509 C20.683.515.501 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D007119 | ||||||
| Scope note: | 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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 79 |
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| History Note: | 79 |
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| DeCS ID: | 7286 | ||||||
| Unique ID: | D007119 | ||||||
| NLM Classification: | WH 700 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1979/01/01 | ||||||
| Date of Entry: | 1978/05/19 | ||||||
| Revision Date: | 2016/05/31 |
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Immunoblastic Lymphadenopathy
- Preferred
| Concept UI |
M0011089 |
| Scope note | 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. |
| Preferred term | Immunoblastic Lymphadenopathy |
| Entry term(s) |
Angioimmunoblastic Lymphadenopathies Angioimmunoblastic Lymphadenopathy Immunoblastic Lymphadenopathies Lymphadenopathies, Angioimmunoblastic Lymphadenopathies, Immunoblastic Lymphadenopathy, Angioimmunoblastic Lymphadenopathy, Immunoblastic |
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