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Erschienen in: European Journal of Pediatrics 8/2008

01.08.2008 | Original Paper

Blue rubber bleb nevus syndrome with simultaneous neurological and skeletal involvement

verfasst von: Meropi S. Tzoufi, Polyxeni Sixlimiri, Iliada Nakou, Maria I. Argyropoulou, Constantinos J. Stefanidis, Antigone Siamopoulou-Mavridou

Erschienen in: European Journal of Pediatrics | Ausgabe 8/2008

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Abstract

Blue rubber bleb nevus syndrome (BRBNS) is a rare disorder characterized by venous malformations usually affecting the skin and the gastrointestinal tract. These skin haemangiomas are present at birth and deteriorate as the body grows, causing primarily cosmetic problems. The haemangiomas of the gastrointestinal tract may appear later in life and may bleed, causing chronic anaemia, or may present with severe complications such as rupture, intestinal torsion, and intussusception. Other organs may also be involved. This article describes a 13-year-old boy with multiple haemangiomas of the skin, the mucous membranes, and the gastrointestinal tract, which caused anaemia and ileoileic intussusception. In this patient, the nervous system was significantly affected with a haemangioma of the left occipital lobe, with complications of stroke. He also had multiple paravertebral heamangiomas, which caused pressure signs and symptoms. This boy suffered from complex partial and generalized seizures and cerebral palsy. Multiple skeletal anomalies were also present from birth. In the relevant literature, this is the first case of BRBNS with simultaneous neurological and skeletal involvement. Such cases should be recognized early, as they can lead to serious multiple health problems and handicaps.
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Metadaten
Titel
Blue rubber bleb nevus syndrome with simultaneous neurological and skeletal involvement
verfasst von
Meropi S. Tzoufi
Polyxeni Sixlimiri
Iliada Nakou
Maria I. Argyropoulou
Constantinos J. Stefanidis
Antigone Siamopoulou-Mavridou
Publikationsdatum
01.08.2008
Verlag
Springer-Verlag
Erschienen in
European Journal of Pediatrics / Ausgabe 8/2008
Print ISSN: 0340-6199
Elektronische ISSN: 1432-1076
DOI
https://doi.org/10.1007/s00431-007-0615-8

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