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Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation.

Publication ,  Journal Article
Veerapandiyan, A; Chinn, IK; Schoch, K; Maloney, KA; Shashi, V
Published in: Eur J Med Genet
2011

We report an adult male with 22q11.2 deletion syndrome and a germline BRCA2 mutation who developed T-cell monoclonal lymphoid proliferation involving the skin and a polyclonal proliferation of a retroperitoneal lymph node without any identifiable infectious and inflammatory causes. This is the first report of reactive lymphoid hyperplasia in the setting of co-occurrence of 22q11.2 deletion syndrome and a BRCA2 mutation. Further cases with a similar presentation should be reported and studies should be directed to identify the possible mechanisms involved.

Duke Scholars

Published In

Eur J Med Genet

DOI

EISSN

1878-0849

Publication Date

2011

Volume

54

Issue

1

Start / End Page

63 / 66

Location

Netherlands

Related Subject Headings

  • Young Adult
  • Syndrome
  • Skin
  • Pseudolymphoma
  • Mutation
  • Male
  • Lymph Nodes
  • Humans
  • Genetics & Heredity
  • Chromosomes, Human, Pair 22
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Veerapandiyan, A., Chinn, I. K., Schoch, K., Maloney, K. A., & Shashi, V. (2011). Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation. Eur J Med Genet, 54(1), 63–66. https://doi.org/10.1016/j.ejmg.2010.09.004
Veerapandiyan, Aravindhan, Ivan Kingyue Chinn, Kelly Schoch, Kristin A. Maloney, and Vandana Shashi. “Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation.Eur J Med Genet 54, no. 1 (2011): 63–66. https://doi.org/10.1016/j.ejmg.2010.09.004.
Veerapandiyan A, Chinn IK, Schoch K, Maloney KA, Shashi V. Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation. Eur J Med Genet. 2011;54(1):63–6.
Veerapandiyan, Aravindhan, et al. “Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation.Eur J Med Genet, vol. 54, no. 1, 2011, pp. 63–66. Pubmed, doi:10.1016/j.ejmg.2010.09.004.
Veerapandiyan A, Chinn IK, Schoch K, Maloney KA, Shashi V. Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation. Eur J Med Genet. 2011;54(1):63–66.
Journal cover image

Published In

Eur J Med Genet

DOI

EISSN

1878-0849

Publication Date

2011

Volume

54

Issue

1

Start / End Page

63 / 66

Location

Netherlands

Related Subject Headings

  • Young Adult
  • Syndrome
  • Skin
  • Pseudolymphoma
  • Mutation
  • Male
  • Lymph Nodes
  • Humans
  • Genetics & Heredity
  • Chromosomes, Human, Pair 22