Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2013 Apr 19:2013:bcr2013008800.
doi: 10.1136/bcr-2013-008800.

Challenges in orthopaedic management of Parkes-Weber syndrome

Affiliations
Case Reports

Challenges in orthopaedic management of Parkes-Weber syndrome

Mara Silva Ferreira et al. BMJ Case Rep. .

Abstract

A 16-year-old boy with a diagnosis of Parkes-Weber syndrome presented with a lower leg discrepancy of 3 cm for orthopaedic management. He had the triad of red skin lesion, lymphoedema and overgrowth of the right leg and multiple arteriovenous fistulae confirmed by angiography. Considering the risk of aggravating the vascular lesion, we decided conservative management of unequal limb lengths as long as this is well tolerated.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Lower limb MRI showing dilated vascular structures in the right lower limb involving subcutaneous and multiple muscle compartments, flow voids consistent with arteriovenous malformation and subcutaneous oedema.
Figure 2
Figure 2
Hypertrophy and trophic cutaneous lesions of the right lower limb.
Figure 3
Figure 3
Hypertrophy of muscles and bones of the right lower limb, with discrepancy of 3 cm.

Similar articles

References

    1. Meier S. Klippel-Trenaunay syndrome: a case study. Adv Neonatal Care 2009;2013:120–4 - PubMed
    1. Samimi M, Lorette E. Klippel-Trenaunay syndrome. Presse Med 2010;2013:487–94 - PubMed
    1. Boon LM, Mulliken JB, Vikkula M. RASA1: variable phenotype with capillary and arteriovenous malformations. Curr Opin Genet Dev 2005;2013:265–9 - PubMed
    1. Brouillard P, Vikkula M. Genetic causes of vascular malformations. Hum Mol Genet 2007;2013(R2):140–9 - PubMed
    1. Renard D, Campello C, Taieb G, et al. Neurological and vascular abnormalities in Klippel-Trenaunay-Weber syndrome. JAMA Neurol 2013;2013;127–8 - PubMed

Publication types