Bannayan-Riley-Ruvalcaba Syndrome in a Patient with a PTEN Mutation Identified by Chromosomal Microarray Analysis: A Case Report
0
조회
0
다운로드
1
인용
0
참고문헌
키워드
초록
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is one of the phosphatase and tensin homolog hamartoma tumor syndrome with a PTEN gene mutation. It is a rare dominant autosomal disorder characterized by cutaneous lipomas, macrocephaly, intestinal polyps, and developmental delay. Diagnosing this syndrome is important, because it may represent the pediatric phenotype of Cowden syndrome, in which there is an increased risk for malignant tumors in children. Until now, the prevalence of BRRS is unknown. Several dozen cases have been reported in the medical literature, but no case has been reported in Korea. Here we report a case of a 19-year-old girl who was diagnosed with BRRS because of macrocephaly, intellectual disability, and intestinal polyps. Her mother had similar findings and a PTEN mutation. Neither patient had mutations detected by conventional mutation-detection techniques, but a PTEN gene deletion was demonstrated by chromosomal microarray analysis.
Abstract
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is one of the phosphatase and tensin homolog hamartoma tumor syndrome with a PTEN gene mutation. It is a rare dominant autosomal disorder characterized by cutaneous lipomas, macrocephaly, intestinal polyps, and developmental delay. Diagnosing this syndrome is important, because it may represent the pediatric phenotype of Cowden syndrome, in which there is an increased risk for malignant tumors in children. Until now, the prevalence of BRRS is unknown. Several dozen cases have been reported in the medical literature, but no case has been reported in Korea. Here we report a case of a 19-year-old girl who was diagnosed with BRRS because of macrocephaly, intellectual disability, and intestinal polyps. Her mother had similar findings and a PTEN mutation. Neither patient had mutations detected by conventional mutation-detection techniques, but a PTEN gene deletion was demonstrated by chromosomal microarray analysis.
참고문헌 (19)
- Buisson P, "Cutaneous lipoma in children:5 cases with Bannayan-Riley-Ruvalcaba syndrome", J Pediatr Surg, 41, pp.1601~1603 (2006)
- Schreibman IR, "The hamartomatous polyposis syndromes: a clinical and molecular review", Am J Gastroenterol, 100, pp.476~490 (2005)
- Bannayan GA, "Lipomatosis, angiomatosis, and macrencephalia. A previously undescribed congenital syndrome", Arch Pathol, 92, pp.1~5 (1971)
- "Bannayan-Riley-Ruvalcaba syndrome" (2012)[URL]
- "Cowden syndrome" (2012)[URL]
- Blumenthal GM, "PTEN hamartoma tumor syndromes", Eur J Hum Genet, 16, pp.1289~1300 (2008)
- Marsh DJ, "Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation", Hum Mol Genet, 7, pp.507~515 (1998)
- Parisi MA, "The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome", J Med Genet, 38, pp.52~58 (2001)
- Latiff ZA, "Bannayan Riley Ruvalcaba syndrome", Ann Acad Med Singap, 39, pp.578~582 (2010)
- Lachlan KL, "Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers", J Med Genet, 44, pp.579~585 (2007)
- Hobert JA, "PTEN hamartoma tumor syndrome:an overview", Genet Med, 11, pp.687~694 (2009)
- Gontijo GM, "Bannayan-Riley-Ruvalcaba syndrome with deforming lipomatous hamartomas in infant--case report", An Bras Dermatol, 88, pp.982~985 (2013)
- Zhou XP, "Germline PTEN promoter mutations and deletions in Cowden", Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase, Am J Hum Genet, pp.2003, 73[DOI]
- "PTEN hamartoma tumor syndrome (PHTS), In GeneReviews" (2001)[URL]
- Shaffer LG, "Using microarray-based molecular cytogenetic methods to identify chromosome abnormalities", Pediatr Ann, 38, pp.440~447 (2009)
- Menko FH, "Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes", Clin Genet, 74, pp.145~154 (2008)
- 서을주, "염색체 Microarray 검사의 임상적 적용", 대한의학유전학회지, 7(2), pp.111~118 (2010), 대한의학유전학회
- Manning M, "Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities", Genet Med, 12, pp.742~745 (2010)
- Miller DT, "Consensus statement:chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies", Am J Hum Genet, 86, pp.749~764 (2010)
