A 13-year-old male child with no prior history presented to the pediatric emergency room for a lesion on the anterior aspect of his left leg associated with pain throughout the limb. On clinical examination, significant hypertrophy of the left lower limb was noted. In the thigh and calf of the same limb, several veins were prominent, enlarged following a tortuous course. The lesion in question, located on the lower part of the medial aspect of the leg, was rounded, with loss of substance, minimally oozing, and clean, without necrosis or associated signs of ischemia. The femoral, popliteal, and pedal pulses were present and symmetrical with the contralateral pulses. The right lower limb was unharmed. The cardiac examination found no murmur or added noise or signs of heart failure. The mucocutaneous examination did not reveal any abnormalities, notably no angiomas. A Doppler ultrasound was performed, revealing multiple arteriovenous communications. The assessment was completed by a CT angiography of the left lower limb, which confirmed high-flow arteriovenous malformations with thrombosis of the left internal iliac vein and the left superficial femoral vein, consistent with Parkes-Weber syndrome. The CT scan also noted skeletal hypertrophy of the left lower limb with muscular hypertrophy and thickening of the soft tissues of the left leg with skin irregularity and loss of substance in the middle third, suggesting an ulcer. The patient was put on anticoagulant treatment with local treatment of his ulcer using 10% povidone iodine and petroleum jelly. The course was marked by an improvement in the ulcer lesion and disappearance of the pain.

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Corresponding author
Leila Debono, Pediatric's Medical Emergency, Children's Hospital of Rabat, Rabat, Morocco (leila.debono@gmail.com)