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Frequent mutations in SH2D1A (XLP) in males presenting with high-grade mature B-cell neoplasms

  • J. T. Sandlund
  • , S. A. Shurtleff
  • , M. Onciu
  • , E. Horwitz
  • , W. Leung
  • , V. Howard
  • , R. Rencher
  • , M. E. Conley

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)E85-E87
JournalPediatric Blood and Cancer
Volume60
Issue number9
DOIs
StatePublished - Sep 2013

Keywords

  • B cells
  • EBV
  • Lymphoma
  • XLP

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