• 1

    Dittus C, Streiff M, Ansell J: Bleeding and clotting in hereditary hemorrhagic telangiectasia. World J Clin Cases 3: 330, 2015.

    • Crossref
    • PubMed
    • Web of Science
    • Search Google Scholar
    • Export Citation
  • 2

    Garg N, Khunger M, Gupta A, et al: Optimal management of hereditary hemorrhagic telangiectasia. J Blood Med 5: 206, 2014.

  • 3

    Govani F, Shovlin C: Hereditary haemorrhagic telangiectasia: a clinical and scientific review. Eur J Hum Genet 17: 860, 2009.

    • Crossref
    • PubMed
    • Web of Science
    • Search Google Scholar
    • Export Citation
  • 4

    Shovlin CL, Guttmacher AE, Buscarini E, et al: Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 91: 66, 2000.

    • Crossref
    • PubMed
    • Search Google Scholar
    • Export Citation
  • 5

    Botella L, Albinana V, Ojeda-Fernandez L, et al: Research on potential biomarkers in hereditary hemorrhagic telangiectasia. Front Genet 6: 115, 2015.

    • Crossref
    • PubMed
    • Web of Science
    • Search Google Scholar
    • Export Citation
  • 6

    Hunt K, Kissel R, Vidal L: Progressive widespread cutaneous telangiectasias. AMA Dermatol 150: 1103, 2014.

  • 7

    McDonald J, Wooderchak W, Whitehead K, et al: Hereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new era. Front Genet 6: 8, 2015.

    • Crossref
    • Web of Science
    • Search Google Scholar
    • Export Citation
  • 8

    Boza JC, Dorn T, Oliveira FB, et al: Case for diagnosis: hereditary hemorrhagic telangiectasia. An Bras Dermatol 89: 999, 2014.

A Case Report of Hereditary Hemorrhagic Telangiectasia Diagnosed in a Podiatric Medical Patient

Kunal Amin Department of Surgery, Saint Barnabas Medical Center, Livingston, NJ.

Search for other papers by Kunal Amin in
Current site
Google Scholar
PubMed
Close
 DPM
and
Douglas Mckay Department of Surgery, Saint Barnabas Medical Center, Livingston, NJ.

Search for other papers by Douglas Mckay in
Current site
Google Scholar
PubMed
Close
 DPM
View More View Less

Hereditary hemorrhagic telangiectasia (HHT), which is also known as Osler-Weber-Rendu syndrome, is a group of related disorders characterized by the development of arteriovenous malformations. These malformations occur in almost all organs but predominantly in the skin, intestines, liver, lungs, and brain. This is a case report of a patient with cutaneous manifestations of HHT in the lower extremities as diagnosed by his podiatric physician. To our knowledge, the literature does not present any case reports in which cutaneous manifestations of the lower extremities followed by a further work-up allowed a diagnosis of HHT.

Corresponding author: Kunal Amin, DPM, Department of Surgery, Saint Barnabas Medical Center, 94 Old Short Hills Rd, Livingston, NJ 07039. (E-mail: kmans009@gmail.com)
Save