Parkes Weber syndrome. Case report.

Authors

  • Dr. Sariwana
  • F. Tabri
  • W. Widita
  • S. Wahab
  • N. Latief
  • S. Budhiani

DOI:

https://doi.org/10.26326/2281-9649.29.2.1966

Keywords:

Arteriovenous malformation, Parkes Weber syndrome, Vascular malformation

Abstract

Parkes Weber syndrome is a rare vascular malformation characterized by arteriovenous malformations, varicose veins and soft tissue hypertrophy of a limb. The diagnosis is confirmed by color doppler ultrasound that highlights vascular malformations, standard X-ray showing the limb volume variation and possible osteolytic lesions, and angiography or magnetic resonance imaging that make evident the damage of the blood vessels and the hypertrophy of the soft tissue. A case characterized by painful vascular malformations and hypertrophy of the left lower limb was here described for its rarity and to underline the need for appropriate investigations aimed at avoiding diagnostic errors and preventing further aggravation of symptoms.

Published

2019-06-06

How to Cite

Sariwana, D., Tabri, F., Widita, W., Wahab, S., Latief, N., & Budhiani, S. (2019). Parkes Weber syndrome. Case report. European Journal of Pediatric Dermatology, 29(2), 70–73. https://doi.org/10.26326/2281-9649.29.2.1966

Issue

Section

Original articles