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Jacob, A.G., Driscoll, D.J., Shaughnessy, W.J., Stanson, A.W., Clay, R.P. and Gloviczki, P. (1998) Klippel Trénaunay Syndrome: Spectrum and Management. Mayo Clinic Proceedings, 73, 28-36.

has been cited by the following article:

• TITLE: Klippel-Trenaunay Syndrome: A Rare Cause of Vaginal Bleeding in the Prepubescent Girl

  AUTHORS: Laila Essabar, Siham Amenzouy, Fatima Zohra Oudghiri, Lamia Kerboubi, Badr Sououd Benjelloun Dakhama

  KEYWORDS: Klippel Trenaunay Syndrome, Vascular Malformation, Soft Tissue Hypertrophy, Genital Bleeding, Child

  JOURNAL NAME: Journal of Biosciences and Medicines, Vol.4 No.11, November 4, 2016

  ABSTRACT: Klippel-Trénaunay syndrome (KTS) is an uncommon congenital disorder with unknown etiology that consists of mixed vascular malformations. Visceral organs may also be involved leading to a variety of manifestations. Although seemingly uncommon, genital tract involvement can occur and be a source of significant morbidity. We hereby describe a case of KTS of a 7-year-old female patient presenting with genital bleeding, large venous and capillary malformations and soft tissue hypertrophy of right limb. Patient was treated conservatively and asked to follow-up regularly. KTS should be kept on mind as a cause of vaginal bleeding in preteen girls especially those with suggestive clinical features. Management of this complex condition is challenging because of its progressive nature and wide range of disease severity.