Gorhamstout syndrome is a rare disorder of unknown etiology characterized by intraosseous proliferation of fibrovascular or lymphatic tissue that results in progressive osteolysis and bone destruction. Is the waitandsee approach in gorham syndrome a therapeutic option. There may be disseminated affeccion or a progressive bone lysis by lymphocytic infil. It is characterized by proliferation of vascular channels that causes destruction and reabsorption of the bone matrix. Volume 46, issue 3, julyseptember 2012, pages 239242. Is a malformation characterized by nonneoplastic lymphoid proliferation, affecting soft tissues and bone. Existem aproximadamente 200 casos reportados na literatura. Jan 14, 2015 to describe our experience using balloon vertebroplasty with polymethylmethacrylate filler in a 10yearold boy with gorhamstout syndrome. Symtoms may include pain, swelling, and increased risk of fracture. To describe our experience using balloon vertebroplasty with polymethylmethacrylate filler in a 10yearold boy with gorhamstout syndrome. Poster actions add bookmark contact presenter send to a friend download pdf. It may affect any part of the skeleton, but most commonly involves the skull, collarbone.
Pdf gorhamstout syndrome is an extremely rare pathology, of unknown etiology. Gorhams disease genetic and rare diseases information. Vertebroplasty in a 10yearold boy with gorhamstout. Puede afectar a cualquier hueso del esqueleto, siendo.