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- Publisher Website: 10.1002/pbc.24525
- Scopus: eid_2-s2.0-84880326475
- PMID: 23589280
- WOS: WOS:000321703900057
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Article: Frequent mutations in SH2D1A (XLP) in males presenting with high-grade mature B-cell neoplasms
Title | Frequent mutations in SH2D1A (XLP) in males presenting with high-grade mature B-cell neoplasms |
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Authors | |
Keywords | Lymphoma XLP EBV B cells |
Issue Date | 2013 |
Citation | Pediatric Blood and Cancer, 2013, v. 60, n. 9, p. E85-E87 How to Cite? |
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. © 2013 Wiley Periodicals, Inc. |
Persistent Identifier | http://hdl.handle.net/10722/294466 |
ISSN | 2023 Impact Factor: 2.4 2023 SCImago Journal Rankings: 0.992 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Sandlund, J. T. | - |
dc.contributor.author | Shurtleff, S. A. | - |
dc.contributor.author | Onciu, M. | - |
dc.contributor.author | Horwitz, E. | - |
dc.contributor.author | Leung, W. | - |
dc.contributor.author | Howard, V. | - |
dc.contributor.author | Rencher, R. | - |
dc.contributor.author | Conley, M. E. | - |
dc.date.accessioned | 2020-12-03T08:22:48Z | - |
dc.date.available | 2020-12-03T08:22:48Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | Pediatric Blood and Cancer, 2013, v. 60, n. 9, p. E85-E87 | - |
dc.identifier.issn | 1545-5009 | - |
dc.identifier.uri | http://hdl.handle.net/10722/294466 | - |
dc.description.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. © 2013 Wiley Periodicals, Inc. | - |
dc.language | eng | - |
dc.relation.ispartof | Pediatric Blood and Cancer | - |
dc.subject | Lymphoma | - |
dc.subject | XLP | - |
dc.subject | EBV | - |
dc.subject | B cells | - |
dc.title | Frequent mutations in SH2D1A (XLP) in males presenting with high-grade mature B-cell neoplasms | - |
dc.type | Article | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1002/pbc.24525 | - |
dc.identifier.pmid | 23589280 | - |
dc.identifier.pmcid | PMC4758190 | - |
dc.identifier.scopus | eid_2-s2.0-84880326475 | - |
dc.identifier.volume | 60 | - |
dc.identifier.issue | 9 | - |
dc.identifier.spage | E85 | - |
dc.identifier.epage | E87 | - |
dc.identifier.eissn | 1545-5017 | - |
dc.identifier.isi | WOS:000321703900057 | - |
dc.identifier.issnl | 1545-5009 | - |