CASE OF PHACOMATOSIS IN A CHILD
DOI:
https://doi.org/10.11603/24116-4944.2018.1.8440Keywords:
bone osteoporosis, fractures, nevus, hereditary.Abstract
The article describes the clinical case of rare Klippel-Trenaunay-Weber syndrome, which is congenital vascular anomaly, named phacomatosis. Despite the literature data, there is significant difficulties of timely diagnosis and treatment of this pathology. The article describes the main clinical and morphological characteristics of this syndrome. The given clinical case confirms the multiple diseases, vessels, and muscle tissues, bones, described in this disease. Pathological pituitary changes detected in a patient with magnetic resonance imaging obviously are also congenital and genetically determined. The uniqueness of the described case is that vascular manifestations are localized on the right hand and bone changes on the opposite limb, which is not typical for this syndrome. Vascular manifestations have noticed four years ago, which, from a small spot, sprawled all over the arm, partially capturing the neck and chest, which is a sign of malignant disease.References
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