Preferred Label : Nasal Type Extranodal NK/T-Cell Lymphoma;
NCIt synonyms : Angiocentric T-Cell Lymphoma; Nasal Type Extranodal NK T-Cell Lymphoma; Extranodal NK/T-Cell Lymphoma;
NCIt related terms : Extranodal NK/T lymphoma-nasal; RETICULOSIS, MALIGNANT; Extranodal NK/T-cell lymphoma, nasal type; NK/T-cell lymphoma, nasal and nasal-type; T/NK-cell lymphoma;
NCIt definition : An aggressive, predominantly extranodal, mature T-cell non-Hodgkin lymphoma. It is
characterized by an often angiocentric and angiodestructive cellular infiltrate composed
of EBV positive NK/T cells. The nasal cavity is the most common site of involvement.
Patients often present with midfacial destructive lesions (lethal midline granuloma).
The disease may disseminate rapidly to various anatomic sites including the gastrointestinal
tract, skin, testis, and cervical lymph nodes. It is also known as angiocentric T-cell
lymphoma. The term polymorphic reticulosis has been widely used to describe the morphologic
changes seen in this type of lymphoma. However, the latter term may also apply to
lymphomatoid granulomatosis, which is an angiocentric and angiodestructive EBV positive
B-cell lymphoproliferative disorder.;
Alternative definition : CDISC: A malignant lymphoid neoplasm composed of EBV-positive NK/T cells arranged
in an angiocentric pattern.;
Neoplastic status : Malignant;
ICD-O code : 9719/3;
Codes from synonyms : 10065855; C86.0;
Origin ID : C4684;
UMLS CUI : C0392788;
Automatic exact mappings (from CISMeF team)
Currated CISMeF NLP mapping
DO Cross reference
Disease excludes abnormal cell
Disease excludes normal cell origin
Disease may have findings
Excludes anatomical site(s)
Has associated anatomic sites
Semantic type(s)
UMLS correspondences (same concept)
Validated automatic mappings to NTBT
concept_is_in_subset
disease_excludes_finding
disease_has_abnormal_cell
disease_has_finding
disease_has_normal_cell_origin
disease_has_normal_tissue_origin
disease_has_primary_anatomic_site
disease_may_have_abnormal_cell
disease_may_have_associated_disease
disease_may_have_cytogenetic_abnormality
disease_may_have_normal_cell_origin
may_be_associated_disease_of_disease