About: Lymphomatoid Granulomatosis     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Lymphomatoid Granulomatosis
equivalentClass
Concept_In_Subset
Semantic_Type
  • Neoplastic Process
Preferred_Name
  • Lymphomatoid Granulomatosis
UMLS_CUI
  • C0024307
Contributing_Source
  • CTEP
ALT_DEFINITION
  • Destructive growth of lymph cells, usually involving the lungs, skin, kidneys, and central nervous system. Grades I and II are not considered cancerous, but grade III is considered a lymphoma.NCI-GLOSS
ICD-O-3_Code
  • 9766/1
Neoplastic_Status
  • Malignant
Legacy_Concept_Name
  • Lymphomatoid_Granulomatosis
FULL_SYN
  • Lymphomatoid granulomatosisPTCTEP10025325
  • LYGABNCI
  • Lymphomatoid GranulomatosisSYNCITCGA
  • Lymphomatoid GranulomatosisPTNCI
  • lymphomatoid granulomatosisPTNCI-GLOSSCDR0000045766
DEFINITION
  • An angiocentric and angiodestructive lymphoproliferative disease involving extranodal sites, comprised of Epstein-Barr virus (EBV)-positive B-cells admixed with reactive T-cells. Incidence is higher among adult males; patients with a history of immunodeficiency are at increased risk. The most common site of involvement is the lung; other common sites include brain, kidney, liver, and skin. Morphologically, three grades are recognized: grade I, II, and III. Grade III lymphomatoid granulomatosis should be approached clinically as a subtype of diffuse large B-cell lymphoma.NCI
code
  • C7930
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