Диссеминированная ювенильная ксантогранулема у взрослых. Клиническое наблюдение

The juvenile xanthogranuloma (Erdheim-Chester disease) is non-Langergans cell histiocytosis. JXG is a rare bening histiocytic disorder. JXG may be present at birth or arise in infancy. Adult onset is reported infrequently. We present a 33-years old woman with deep juvenile xanthogranuloma.