Literature DB >> 27358095

Assessment of PTEN-associated vascular malformations in a patient with Bannayan-Riley-Ruvalcaba syndrome.

Sandra Anusic1, Robert Karl Josef Clemens1, Thomas Oleg Meier1, Beatrice Ruth Amann-Vesti1.   

Abstract

Misdiagnosis of phosphatase and tensin homologue hamartoma syndromes is common. Correct diagnosis has a relevant impact on patients, as the risk of malignancies is high and treatment options are limited. We report the case of a 24-year-old man who presented with symptomatic vascular intramuscular lesions of the left forearm and right calf, macrocephaly, post Hashimoto thyroiditis, a multicystic intracranial paratrigonal lesion, lentiginous hyperpigmented maculae on the foreskin and multiple skin lesions. MRI showed extended fibrofatty changes and malformed vessels in the forearm and calf lesions, also, arteriovenous shunting was present in these lesions. The patient had been treated by embolisation and surgically in the past, with limited results. A multidisciplinary assessment and genetic counselling were undertaken and a surveillance programme was initiated. Treatment options of the symptomatic vascular lesions include excision or possibly cryoablation. Physiotherapy to prevent progression of the contractures should be initiated meanwhile. 2016 BMJ Publishing Group Ltd.

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Year:  2016        PMID: 27358095      PMCID: PMC4932365          DOI: 10.1136/bcr-2016-215188

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


  24 in total

1.  Diagnosis of Proteus syndrome was correct.

Authors:  Edwin P Kirk; Janine M Smith; Michael Field; Glenn M Marshall; Deborah J Marsh
Journal:  Am J Med Genet A       Date:  2004-10-01       Impact factor: 2.802

2.  PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.

Authors:  Kyle C Kurek; Emily Howard; L B Tennant; Joseph Upton; Ahmad I Alomari; Patricia E Burrows; Kim Chalache; David J Harris; Cameron C Trenor; Charis Eng; Steven J Fishman; John B Mulliken; Antonio R Perez-Atayde; Harry P W Kozakewich
Journal:  Am J Surg Pathol       Date:  2012-05       Impact factor: 6.394

3.  PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol.

Authors:  Maria Piccione; Tiziana Fragapane; Vincenzo Antona; Daniela Giachino; Francesco Cupido; Giovanni Corsello
Journal:  Am J Med Genet A       Date:  2013-10-07       Impact factor: 2.802

4.  Lipomatosis, angiomatosis, and macrencephalia. A previously undescribed congenital syndrome.

Authors:  G A Bannayan
Journal:  Arch Pathol       Date:  1971-07

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
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6.  Bannayan-Riley-Ruvalcaba syndrome.

Authors:  R J Gorlin; M M Cohen; L M Condon; B A Burke
Journal:  Am J Med Genet       Date:  1992-10-01

7.  Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity.

Authors:  Frédéric Caux; Henri Plauchu; Frédéric Chibon; Laurence Faivre; Olivier Fain; Pierre Vabres; Françoise Bonnet; Zied Ben Selma; Liliane Laroche; Marion Gérard; Michel Longy
Journal:  Eur J Hum Genet       Date:  2007-03-28       Impact factor: 4.246

8.  Characterization of a distinct syndrome that associates complex truncal overgrowth, vascular, and acral anomalies: a descriptive study of 18 cases of CLOVES syndrome.

Authors:  Ahmad I Alomari
Journal:  Clin Dysmorphol       Date:  2009-01       Impact factor: 0.816

9.  Genetic/familial high-risk assessment: breast and ovarian, version 1.2014.

Authors:  Mary B Daly; Robert Pilarski; Jennifer E Axilbund; Saundra S Buys; Beth Crawford; Susan Friedman; Judy E Garber; Carolyn Horton; Virginia Kaklamani; Catherine Klein; Wendy Kohlmann; Allison Kurian; Jennifer Litton; Lisa Madlensky; P Kelly Marcom; Sofia D Merajver; Kenneth Offit; Tuya Pal; Boris Pasche; Gwen Reiser; Kristen Mahoney Shannon; Elizabeth Swisher; Nicoleta C Voian; Jeffrey N Weitzel; Alison Whelan; Georgia L Wiesner; Mary A Dwyer; Rashmi Kumar
Journal:  J Natl Compr Canc Netw       Date:  2014-09       Impact factor: 11.908

10.  The spectrum of vascular anomalies in patients with PTEN mutations: implications for diagnosis and management.

Authors:  Wen-Hann Tan; Hagit N Baris; Patricia E Burrows; Caroline D Robson; Ahmad I Alomari; John B Mulliken; Steven J Fishman; Mira B Irons
Journal:  J Med Genet       Date:  2007-05-25       Impact factor: 6.318

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  1 in total

Review 1.  A Primer on a Comprehensive Genetic Approach to Vascular Anomalies.

Authors:  Alexandra J Borst; Taizo A Nakano; Francine Blei; Denise M Adams; Jessica Duis
Journal:  Front Pediatr       Date:  2020-10-19       Impact factor: 3.418

  1 in total

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