Literature DB >> 25564593

Rare manifestations in a case of Osler-Weber-Rendu disease.

Abhijai Singh1, Vikas Suri2, Sanjay Jain2, Subhash Varma2.   

Abstract

Osler-Weber-Rendu disease (OWRD) is a rare vascular dysplasia that presents most commonly with epistaxis. The most dreaded complication, however, is an intracranial haemorrhage. We present a patient with two rare manifestations of OWRD, subdural haematoma and portal venous hypertension, both seldom reported in the literature. The patient made a full recovery and continues to do well at this time. 2015 BMJ Publishing Group Ltd.

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Year:  2015        PMID: 25564593      PMCID: PMC4289744          DOI: 10.1136/bcr-2014-207852

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


  32 in total

1.  Hereditary haemorrhagic telangiectasia: a genetic and bibliographical study.

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Journal:  Br J Dermatol Syph       Date:  1950 Jul-Aug

2.  Graded contrast echocardiography in pulmonary arteriovenous malformations.

Authors:  J A Parra; J Bueno; J Zarauza; C Fariñas-Alvarez; J M Cuesta; P Ortiz; R Zarrabeitia; A Pérez del Molino; M Bustamante; L M Botella; M T Delgado
Journal:  Eur Respir J       Date:  2009-12-08       Impact factor: 16.671

3.  Multiple cerebral arteriovenous malformations associated with soft-tissue vascular malformations. Case report.

Authors:  A Hanieh; P C Blumbergs; P G Carney
Journal:  J Neurosurg       Date:  1981-05       Impact factor: 5.115

4.  Ocular manifestations in hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease): a case-series.

Authors:  Michele Rinaldi; Elisabetta Buscarini; Cesare Danesino; Flavia Chiosi; Antonella De Benedictis; Antonio Porcellini; Ciro Costagliola
Journal:  Ophthalmic Genet       Date:  2010-12-21       Impact factor: 1.803

Review 5.  Radiologic assessment of brain arteriovenous malformations: what clinicians need to know.

Authors:  Sasikhan Geibprasert; Sirintara Pongpech; Pakorn Jiarakongmun; Manohar M Shroff; Derek C Armstrong; Timo Krings
Journal:  Radiographics       Date:  2010-03       Impact factor: 5.333

6.  Liver disease in patients with hereditary hemorrhagic telangiectasia.

Authors:  G Garcia-Tsao; J R Korzenik; L Young; K J Henderson; D Jain; B Byrd; J S Pollak; R I White
Journal:  N Engl J Med       Date:  2000-09-28       Impact factor: 91.245

7.  The natural history of epistaxis in hereditary hemorrhagic telangiectasia.

Authors:  O S AAssar; C M Friedman; R I White
Journal:  Laryngoscope       Date:  1991-09       Impact factor: 3.325

8.  Antiestrogen therapy for hereditary hemorrhagic telangiectasia: a double-blind placebo-controlled clinical trial.

Authors:  Eitan Yaniv; Michal Preis; Tuvia Hadar; Jacob Shvero; Miriam Haddad
Journal:  Laryngoscope       Date:  2009-02       Impact factor: 3.325

Review 9.  Hereditary haemorrhagic telangiectasia: a clinical and scientific review.

Authors:  Fatima S Govani; Claire L Shovlin
Journal:  Eur J Hum Genet       Date:  2009-04-01       Impact factor: 4.246

10.  Hereditary hemorrhagic telangiectasia: multi-detector row helical CT assessment of hepatic involvement.

Authors:  Amato Antonio Stabile Ianora; Maurizio Memeo; Carlo Sabba; Anna Cirulli; Antonio Rotondo; Giuseppe Angelelli
Journal:  Radiology       Date:  2003-11-26       Impact factor: 11.105

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