Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Más filtros











Base de datos
Intervalo de año de publicación
1.
Am J Clin Pathol ; 140(3): 387-94, 2013 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-23955458

RESUMEN

OBJECTIVES: To examine the usefulness of the MYD88 L265P somatic mutation in identifying cases of lymphoplasmacytic lymphoma (LPL) from other lymphoplasmacytic neoplasms in bone marrow biopsy specimens. METHODS: We studied 64 bone marrow biopsy specimens with involvement by various small B-cell lymphomas or plasma cell myeloma. RESULTS: The MYD88 L265P somatic mutation was present in 13/13 cases of LPL, 1/13 cases of hairy cell leukemia, and absent in the other mature B-cell neoplasms tested. A test set of diagnostically challenging bone marrow cases with lymphoplasmacytoid morphology (B-cell lymphoma, not otherwise specified) was selected for additional review and reclassified, without knowledge of the MYD88 L265P status. Of those 16 cases, 7 were positive for MYD88, including 4/4 cases that were reclassified as LPL during the review. CONCLUSIONS: Although not entirely specific, MYD88 L265P is a useful adjunct for bone marrow diagnosis in separating LPL from other small B-cell lymphomas and plasma cell myeloma.


Asunto(s)
Linfocitos B/patología , Médula Ósea/patología , Trastornos Linfoproliferativos/diagnóstico , Factor 88 de Diferenciación Mieloide/genética , Macroglobulinemia de Waldenström/diagnóstico , Adulto , Anciano , Anciano de 80 o más Años , Linfocitos B/metabolismo , Médula Ósea/metabolismo , Diagnóstico Diferencial , Femenino , Humanos , Linfoma de Células B/diagnóstico , Linfoma de Células B/genética , Linfoma de Células B/metabolismo , Trastornos Linfoproliferativos/genética , Trastornos Linfoproliferativos/metabolismo , Masculino , Persona de Mediana Edad , Mieloma Múltiple/diagnóstico , Mieloma Múltiple/genética , Mieloma Múltiple/metabolismo , Factor 88 de Diferenciación Mieloide/metabolismo , Estudios Retrospectivos , Macroglobulinemia de Waldenström/genética , Macroglobulinemia de Waldenström/metabolismo
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA