thymoma type B1
A thymic epithelial neoplasm characterized by the presence of expanded areas which resemble the normal thymic cortex. The neoplastic epithelial cells are small and scant and there is a dense T-lymphocytic component present. Areas of medullary differentiation with or without Hassall's corpuscles are also present. It may be associated with myasthenia gravis, pure red cell aplasia, and hypogammaglobulinemia. It has a low grade malignant potential. The majority of cases occur in the anterior mediastinum as Masaoka stage I tumors. A minority of the cases occur as stage II tumors. [ NCIT:C6887 ]
Term info
- UMLS:C1266094 (NCIT:C6887)
- ICDO:8583/1 (NCIT:C6887)
- NCIT:C6887 (MONDO:equivalentTo)
- DOID:6917 (MONDO:equivalentTo)
- EFO:1000584 (MONDO:equivalentTo)
A thymic epithelial neoplasm characterized by the presence of expanded areas which resemble the normal thymic cortex. The neoplastic epithelial cells are small and scant and there is a dense T-lymphocytic component present. Areas of medullary differentiation with or without Hassall's corpuscles are also present. It may be associated with myasthenia gravis, pure red cell aplasia, and hypogammaglobulinemia. It has a low grade malignant potential. The majority of cases occur in the anterior mediastinum as Masaoka stage I tumors. A minority of the cases occur as stage II tumors.
http://linkedlifedata.com/resource/umls/id/C1266094, http://purl.obolibrary.org/obo/NCIT_C6887, http://purl.obolibrary.org/obo/DOID_6917
thymoma, organoid, lymphocyte-predominant thymoma, organoid thymoma, predominantly cortical thymoma, lymphocyte-rich thymoma, thymoma type B1
MONDO:0006459