Preferred Label : Stage III Nasopharyngeal Undifferentiated Carcinoma AJCC v7;
NCIt synonyms : Stage III Lymphoepithelioma of the Nasopharynx; Nasopharyngeal Undifferentiated Carcinoma Stage III; Stage III Nasopharyngeal Undifferentiated Carcinoma; Stage III Lymphoepithelioma of Nasopharynx; Stage III Nasopharyngeal Lymphoepithelioma;
NCIt related terms : Stage III Undifferentiated Nasopharyngeal Throat Cancer;
NCIt definition : Stage III includes: (T1, N2, M0); (T2, N2, M0); (T3, N0, M0); (T3, N1, M0); (T3, N2,
M0). T1: Nasopharyngeal cancer with tumor confined to the nasopharynx, or tumor extending
to oropharynx and/or nasal cavity without parapharyngeal extension. Parapharyngeal
extension denotes posterolateral infiltration of tumor. T2: Nasopharyngeal cancer
with parapharyngeal extension. Parapharyngeal extension denotes posterolateral infiltration
of tumor. T3: Nasopharyngeal cancer with tumor involving bony structures of skull
base and/or paranasal sinuses. N0: No regional lymph node metastasis. N1: Nasopharyngeal
cancer with unilateral metastasis in cervical lymph node(s), 6 cm or less in greatest
dimension, above the supraclavicular fossa, and/or unilateral or bilateral, retropharyngeal
lymph nodes, 6 cm or less in greatest dimension. Midline nodes are considered ipsilateral
nodes. N2: Nasopharyngeal cancer with bilateral metastasis in cervical lymph node(s),
6 cm or less in greatest dimension, above the supraclavicular fossa. Midline nodes
are considered ipsilateral nodes. M0: No distant metastasis. (AJCC 7th ed.);
Neoplastic status : Malignant;
Origin ID : C8227;
UMLS CUI : C0280383;
Currated CISMeF NLP mapping
Disease excludes abnormal cell
Disease may have findings
Has associated anatomic sites
Semantic type(s)
UMLS correspondences (same concept)
concept_is_in_subset
disease_excludes_finding
disease_has_abnormal_cell
disease_has_associated_disease
disease_has_finding
disease_has_normal_cell_origin
disease_has_normal_tissue_origin
disease_has_primary_anatomic_site
disease_is_stage
disease_mapped_to_gene
disease_may_have_cytogenetic_abnormality
disease_may_have_molecular_abnormality