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Frequent mutations in SH2D1A (XLP) in males presenting with high-grade mature B-cell neoplasms.
Sandlund, J T; Shurtleff, S A; Onciu, M; Horwitz, E; Leung, W; Howard, V; Rencher, R; Conley, M E.
Afiliación
  • Sandlund JT; Department of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA. john.sandlund@stjude.org
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.
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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

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