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Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation
- Source :
- European journal of medical genetics. 54(1)
- Publication Year :
- 2010
-
Abstract
- 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.
- Subjects :
- Male
Chromosomes, Human, Pair 22
Retroperitoneal Lymph Node
Biology
medicine.disease_cause
Lymphoid hyperplasia
Germline
Young Adult
Pseudolymphoma
DiGeorge syndrome
Genetics
medicine
Humans
Abnormalities, Multiple
Genetics (clinical)
Immunodeficiency
Skin
BRCA2 Protein
Mutation
General Medicine
Syndrome
medicine.disease
Lymphoma
Monoclonal
Cancer research
Lymph Nodes
medicine.symptom
Chromosome Deletion
Subjects
Details
- ISSN :
- 18780849
- Volume :
- 54
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- European journal of medical genetics
- Accession number :
- edsair.doi.dedup.....b76897433cb7daab5a0a244a0651d552