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Indian Pediatr ; 2009 Mar; 46(3): 255-256
Article in English | IMSEAR | ID: sea-12937

ABSTRACT

Gorhams disease, also known as massive osteolysis or vanishing bone disease is an extremely rare bone disease. It is characterized by angiomatosis with adjacent bone resorption. We report an 8-years old boy with the disease who was managed successfully with alpha 2b interferon therapy.


Subject(s)
Child , Chylothorax/etiology , Chylothorax/therapy , Diphosphonates/therapeutic use , Humans , Interferon Type I/therapeutic use , Interferon-alpha , Male , Osteolysis , Osteolysis, Essential/complications , Osteolysis, Essential/diagnosis , Osteolysis, Essential/therapy , Recombinant Proteins
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