Literature DB >> 24474112

Bannayan-Riley-Ruvalcaba syndrome with deforming lipomatous hamartomas in infant--case report.

Gabriela Maria Abreu Gontijo1, Clóvis Antonio Lopes Pinto2, Silvia Regina Rogatto3, Isabela Werneck da Cunha2, Samuel Aguiar4, Célia Antônia Xavier de Moraes Alves5.   

Abstract

Bannayan-Riley-Ruvalcaba Syndrome is a rare condition caused by mutations in the PTEN gene. It displays association of multiple lipomas, macrocephaly, hemangiomas, hamartomatous intestinal polyposis, developmental delay and speckled pigmented maculae on the male genitalia. We report the case of a nine-month-old boy who had fast growing and progressive tumors for three months, macrocephaly and lentigines on the penis. Imaging tests showed extensive lipomatosis with invasion of paraspinal muscles, enlargement of the spinal canal and spinal cord compression; after surgical excision of the mass, the pathology was consistent with lipoma. Adipocyte culture karyotype demonstrated PTEN mutation. We present this case for its rarity and exuberance.

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Year:  2013        PMID: 24474112      PMCID: PMC3900354          DOI: 10.1590/abd1806-4841.20132730

Source DB:  PubMed          Journal:  An Bras Dermatol        ISSN: 0365-0596            Impact factor:   1.896


  9 in total

1.  Bannayan Riley Ruvalcaba syndrome.

Authors:  Zarina Abdul Latiff; Raymond Warouw Atmawidjaja; Raja Juanita RajaLope; Sharifah Azween Syed Omar; Syed Zulkifli Syed Zakaria; Rahman A Jamal
Journal:  Ann Acad Med Singapore       Date:  2010-07       Impact factor: 2.473

2.  Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.

Authors:  D J Marsh; V Coulon; K L Lunetta; P Rocca-Serra; P L Dahia; Z Zheng; D Liaw; S Caron; B Duboué; A Y Lin; A L Richardson; J M Bonnetblanc; J M Bressieux; A Cabarrot-Moreau; A Chompret; L Demange; R A Eeles; A M Yahanda; E R Fearon; J P Fricker; R J Gorlin; S V Hodgson; S Huson; D Lacombe; C Eng
Journal:  Hum Mol Genet       Date:  1998-03       Impact factor: 6.150

Review 3.  An overlap of Cowden's disease and Bannayan-Riley-Ruvalcaba syndrome in the same family.

Authors:  J Perriard; J H Saurat; M Harms
Journal:  J Am Acad Dermatol       Date:  2000-02       Impact factor: 11.527

4.  Clinical and histopathological findings in Bannayan-Riley-Ruvalcaba syndrome.

Authors:  Emel Erkek; Selda Hizel; Cihat Sanlý; A Bulent Erkek; Meryem Tombakoglu; Onder Bozdogan; Sedat Ulkatan; Cengiz Akarsu
Journal:  J Am Acad Dermatol       Date:  2005-10       Impact factor: 11.527

5.  PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.

Authors:  D J Marsh; J B Kum; K L Lunetta; M J Bennett; R J Gorlin; S F Ahmed; J Bodurtha; C Crowe; M A Curtis; M Dasouki; T Dunn; H Feit; M T Geraghty; J M Graham; S V Hodgson; A Hunter; B R Korf; D Manchester; S Miesfeldt; V A Murday; K L Nathanson; M Parisi; B Pober; C Romano; C Eng
Journal:  Hum Mol Genet       Date:  1999-08       Impact factor: 6.150

6.  The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome.

Authors:  M A Parisi; M B Dinulos; K A Leppig; V P Sybert; C Eng; L Hudgins
Journal:  J Med Genet       Date:  2001-01       Impact factor: 6.318

7.  Lifetime cancer risks in individuals with germline PTEN mutations.

Authors:  Min-Han Tan; Jessica L Mester; Joanne Ngeow; Lisa A Rybicki; Mohammed S Orloff; Charis Eng
Journal:  Clin Cancer Res       Date:  2012-01-15       Impact factor: 12.531

Review 8.  PTEN hamartoma tumor syndromes.

Authors:  Gideon M Blumenthal; Phillip A Dennis
Journal:  Eur J Hum Genet       Date:  2008-09-10       Impact factor: 4.246

9.  Bannayan-Riley-Ruvalcaba syndrome: a cause of extreme macrocephaly and neurodevelopmental delay.

Authors:  N E Lynch; S A Lynch; J McMenamin; D Webb
Journal:  Arch Dis Child       Date:  2009-03-25       Impact factor: 3.791

  9 in total
  1 in total

1.  Bannayan-Riley-Ruvalcaba Syndrome in a Patient with a PTEN Mutation Identified by Chromosomal Microarray Analysis: A Case Report.

Authors:  Sun Hwa Lee; Eell Ryoo; Hann Tchah
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2017-03-27
  1 in total

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