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Updated: May 16, 2026

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
[Blue rubber bleb nevus syndrome: A case report]
M V López-Ugalde1, M J Cazares-Méndez, L D Vivar-Aquino
1Departamento de Gastroenterología y Nutrición, Instituto Nacional de Pediatría, México, D.F., México. martha_veronical@hotmail.com
Abstract:
Blue Rubber Bleb Nevus Syndrome (BRBS) is a rare disease, characterized by multiple vascular malformations in the skin and gastrointestinal tract. Other organs can also be affected, presenting different clinical manifestations such as arthralgia, epistaxis, hemoptysis, hematuria, hemothorax, mild thrombocytopenia, consumptive coagulopathy, and bone deformities, among others. We present a case of BRBS in a nine-year-old boy with the characteristic clinical manifestations of punctated purplish-blue skin lesions that vary in size and gastrointestinal vascular malformations with upper digestive tract bleeding.
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