Frequent mutations in SH2D1A (XLP) in males presenting with high-grade mature B-cell neoplasms.
Pediatr Blood Cancer
; 60(9): E85-7, 2013 Sep.
Article
en En
| MEDLINE
| ID: mdl-23589280
X-linked lymphoproliferative syndrome (XLP) is caused by mutations in SH2D1A, and is associated with overwhelming infectious mononucleosis, aplastic anemia, hypogammaglobulinemia, and B-cell lymphomas. However, the frequency of SH2D1A mutations in males who present with B NHL is unknown. Five cases of XLP were diagnosed among 158 males presenting with B NHL (approximately 3.2%). Four of the patients had two episodes of B NHL and one had a single episode of B NHL followed by aggressive infectious mononucleosis. Prospective screening for XLP in males with B-cell lymphoma at the time of initial diagnosis should be considered.
Palabras clave
Texto completo:
1
Base de datos:
MEDLINE
Asunto principal:
Sistema de Registros
/
Péptidos y Proteínas de Señalización Intracelular
/
Trastornos Linfoproliferativos
/
Mutación
Tipo de estudio:
Diagnostic_studies
/
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Límite:
Humans
/
Male
Idioma:
En
Revista:
Pediatr Blood Cancer
Asunto de la revista:
HEMATOLOGIA
/
NEOPLASIAS
/
PEDIATRIA
Año:
2013
Tipo del documento:
Article
País de afiliación:
Estados Unidos