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Diseases

Angiolymphoid hyperplasia

angiolymphoid hyperplasia

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Angiolymphoid hyperplasia
Standard Disease Name
angiolymphoid hyperplasia
MeSH Tree
No data
ICD-10
D47.Z2

Identifiers

DO ID
No data
MeSH ID
D005871
OMIM ID
No data
UMLS ID
C0017531
HPO ID
No data

Description and Extensions

Description
NCI2016_NCI-GLOSS_1602D:A rare disorder in which growths that are benign (not cancer) develop in lymph node tissue.|NCI2016_02D:A disorder characterized by lymphoid hyperplasia in the lymph nodes. There are two histologic variants recognized: the hyaline-vascular type and the plasma cell type. In the hyaline vascular type there are hyalinized vessels present in the lymphoid follicles. In the plasma cell type there is pronounced plasma cell proliferation. Clinically, the disease may be localized; manifested with localized lymphadenopathy, or multicentric; manifested with generalized lymphadenopathy, fever, organomegaly, and sometimes POEMS syndrome. In contrast to patients with localized disease who are usually cured following resection of the lesion, patients with the multicentric form of the disease may follow a progressive clinical course, complicated by infection, Kaposi sarcoma or lymphoma.|MSH2017_2016_08_12:Large benign, hyperplastic lymph nodes. The more common hyaline vascular subtype is characterized by small hyaline vascular follicles and interfollicular capillary proliferations. Plasma cells are often present and represent another subtype with the plasma cells containing IgM and IMMUNOGLOBULIN A.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
04
HLA-C
major histocompatibility complex, class I, C
major histocompatibility complex, class I, C
07
MUC1
mucin 1, cell surface associated
mucin 1, cell surface associated