Literature DB >> 22605600

Proliferative retinopathy in Cowden syndrome.

Qasim Mansoor1, David H W Steel.   

Abstract

Cowden syndrome is a multiple hamartoma syndrome with a high risk of breast and thyroid tumours, both benign and malignant. The authors report a 24-year-old female patient who presented with reduced vision in both eyes. Ocular examination showed vitreous haemorrhage secondary to retinal new vessels in both eyes. There was no evidence of diabetes mellitus, and she had a wide range of normal investigations. She was labelled as idiopathic retinal neovascularisation. Fifteen years later, she presented with a lump in her left breast and a previous history of excision of a benign lump from her right breast. She also reported multiple tumours in her family. Clinical diagnosis of Cowden syndrome was made and genetic testing confirmed mutation of the PTEN gene.

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Year:  2012        PMID: 22605600      PMCID: PMC3316858          DOI: 10.1136/bcr.11.2011.5273

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  5 in total

1.  PTEN modulates vascular endothelial growth factor-mediated signaling and angiogenic effects.

Authors:  Jianhua Huang; Christopher D Kontos
Journal:  J Biol Chem       Date:  2002-01-09       Impact factor: 5.157

Review 2.  Cowden syndrome.

Authors:  A M Hanssen; J P Fryns
Journal:  J Med Genet       Date:  1995-02       Impact factor: 6.318

3.  Cowden disease: gene marker studies and measurements of epidermal growth factor.

Authors:  H E Carlson; T W Burns; S L Davenport; A M Luger; M A Spence; R S Sparkes; D N Orth
Journal:  Am J Hum Genet       Date:  1986-06       Impact factor: 11.025

Review 4.  Cowden syndrome: a critical review of the clinical literature.

Authors:  Robert Pilarski
Journal:  J Genet Couns       Date:  2008-10-30       Impact factor: 2.537

5.  The Cowden syndrome: a clinical and genetic study in 21 patients.

Authors:  T M Starink; J P van der Veen; F Arwert; L P de Waal; G G de Lange; J J Gille; A W Eriksson
Journal:  Clin Genet       Date:  1986-03       Impact factor: 4.438

  5 in total
  3 in total

1.  Intermediate uveitis in a child with phosphatase and tensin homolog gene mutation and Bannayan-Riley-Ruvalcaba syndrome.

Authors:  Daphna Prat; Iris Ben Bassat Mizrachi; Vicktoria Vishnevskia-Dai
Journal:  BMJ Case Rep       Date:  2019-02-12

2.  Corneal confocal microscopy anomalies associated with cowden syndrome: a case report.

Authors:  Sandro Sbordone; Alfonso Savastano; Maria Cristina Savastano; Vito Romano; Mario Bifani; Silvio Savastano
Journal:  Case Rep Ophthalmol       Date:  2013-08-15

3.  Hamartoma-like lesions in the mouse retina: an animal model of Pten hamartoma tumour syndrome.

Authors:  Nobuhiko Tachibana; Yacine Touahri; Rajiv Dixit; Luke Ajay David; Lata Adnani; Robert Cantrup; Tooka Aavani; Rachel O Wong; Cairine Logan; Kyle C Kurek; Carol Schuurmans
Journal:  Dis Model Mech       Date:  2018-05-21       Impact factor: 5.758

  3 in total

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