Cano Bernardo, Insa Sonia, Cifrián Carlos, Cortina Héctor, Hernández Miguel
Servicio de Radiodiagnóstico de adultos, Hospital La Fe, Valencia, España.
Radiologia. 2006 Jan-Feb;48(1):33-6. doi: 10.1016/s0033-8338(06)73127-7.
Gorham-Stout syndrome, also called "disappearing bone disease" or idiopathic massive osteolysis, is a rare disease of unknown etiology and pathogenesis. It is characterized by rapidly progressive localized massive osteolysis associated to a proliferation of vascular structures of benign origin in which the absence of new bone formation is representative. We present two cases (a six-year-old boy with affected right ulna, and a 15-year-old girl with right rib affection associated to chylothorax) of this disease with the characteristic clinical, histological, and imaging findings.
戈勒姆-斯托特综合征，也称为“骨质消失病”或特发性大块骨质溶解症，是一种病因和发病机制不明的罕见疾病。其特征为迅速进展的局限性大块骨质溶解，并伴有良性起源的血管结构增生，其中缺乏新骨形成是其典型表现。我们报告了两例该疾病的病例（一例是右尺骨受累的6岁男孩，另一例是右肋骨受累并伴有乳糜胸的15岁女孩），具有典型的临床、组织学和影像学表现。
