Blue rubber bleb nevus syndrome in Child
BRBNS is rare; only about 200 cases have been described in the literature to date. The cause is unknown. Most cases of BRBNS occur spontaneously, although there have been reports of autosomal dominantly inherited cases. Some evidence suggests that the mutation for some cases may occur on chromosome 9p. Most patients with BRBNS have double (cis) somatic mutations in the TEK gene, which encodes TIE2, an endothelial cell tyrosine kinase receptor.
BRBNS has been reported to occur more frequently in individuals of Northern European descent. It affects males and females equally. Blue rubber bleb nevi are often present at birth or in early childhood, but onset has also been reported in adults. Over time, they increase in size and number. Usually GI involvement becomes evident during young adulthood.
Morbidity and mortality depend on the extent of visceral involvement. Most patients live a normal life span. However, hemorrhage from the GI tract can be fatal. Lesions involving the bones and joints can be uncomfortable and disfiguring and, rarely, require amputation. Rarely, lesions of the central nervous system can be fatal.
Blue rubber bleb nevi have variable clinical appearances and can range from small blue-black punctate papules to large disfiguring tumors. The cutaneous lesions do not bleed spontaneously and do not undergo malignant transformation. GI venous malformations predominantly occur in the small intestines but can occur anywhere from the mouth to the anus. These lesions easily bleed and can result in occult blood loss and iron-deficiency anemia. They can also lead to abdominal pain, intussusception, volvulus, infarction, and internal hemorrhage.
Involvement of other organs may result in menorrhagia, intermittent proptosis, hematuria, epistaxis, hemoptysis, hemothorax, hemopericardium, thrombotic complications, focal seizures, spasticity, ataxia, weakness, arthralgias, decreased range of motion, and deformity.
D18.00 – Hemangioma unspecified site
254784002 – Blue rubber bleb nevus
- Osler-Weber-Rendu disease – visceral and cutaneous lesions are usually smaller (2-5 mm) and punctiform. There can also be subungual lesions, nail-bed involvement, and spider and punctate telangiectasias.
- Maffucci syndrome – bony abnormalities resulting from chondroplasia and defective ossification. There is also a high incidence of malignant transformation.
- Klippel-Trenaunay-Weber syndrome – typically confined to one extremity.
- Von Hippel-Lindau disease
- Sturge-Weber syndrome
- Kaposi sarcoma
- Cobb syndrome
- Venous lakes
- Also included in the differential are eccrine spiradenoma, glomus tumor, glomangioma, angiolipoma, angioleiomyoma, angiosarcoma, and leiomyoma.