Thalidomide as an effective treatment in a case of Osler Weber Rendu syndrome: a case report

Authors

  • Titli Bandyopadhyay Senior Resident, Department of ENT, IQ City Medical College, Durgapur, West Bengal http://orcid.org/0000-0001-8819-8565
  • VT Anand Consultant, Department of ENT, Manipal Hospital, Bangalore, Karnataka
  • Dibyendu Gangopadhyay Tutor, Department of Microbiology, Gouri Devi Institue of Medical Sciences and Hospital, Durgapur, West Bengal

DOI:

https://doi.org/10.3126/ajms.v7i4.14554

Keywords:

Epistaxis, Hereditary haemorrhagic telangiectasia, Thalidomide

Abstract

Osler Weber Rendu Syndrome (OWRS), or Hereditary Hemorrhagic telangiectasia (HHT) is an autosomal dominant disease presents with epistaxis, telangiactesia and multiorgan vascular dysplasia. Recurrent epistaxis is common in these patients and various local forms of therapy is tried to treat the condition, but there is lack of definitive and effective treatment. We present a patient of HHT with severe recurrent epistaxis successfully treated with thalidomide.

Asian Journal of Medical Sciences Vol.7(4) 2016 107-109

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Published

2016-07-04

How to Cite

Bandyopadhyay, T., Anand, V., & Gangopadhyay, D. (2016). Thalidomide as an effective treatment in a case of Osler Weber Rendu syndrome: a case report. Asian Journal of Medical Sciences, 7(4), 107–109. https://doi.org/10.3126/ajms.v7i4.14554

Issue

Vol. 7 No. 4 (2016)

Section

Case Reports

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