Bisagni-Faure A, Giraudet-Le Quintrec J S, Job-Deslandre C, Menkes C J
Service de Rhumatologie, Hôpital Cochin, Paris.
Ann Med Interne (Paris). 1991;142(1):17-20.
Disappearing bone disease is a rare syndrome, characterized by an idiopathic and spontaneous progressive resorption of bone, for which different etiologies must be considered. The classification of this disease is difficult; acro-osteolysis involves the phalanges or the carpus and tarsus. Massive osteolysis corresponds to diffuse multicentric cystic hemangiomatosis and Gorham and Stout's disease. We describe two cases of acro-osteolysis and one of Gorham and Stout's disease. The mechanism of disappearing bone disease remains unknown and no treatment has yet been found to stop its evolution.
骨质溶解症是一种罕见的综合征，其特征为特发性、自发性的进行性骨质吸收，对此必须考虑不同的病因。这种疾病的分类很困难；肢端骨质溶解累及指骨或腕骨和跗骨。大块骨质溶解相当于弥漫性多中心囊性血管瘤病以及戈勒姆病和斯托特病。我们描述了两例肢端骨质溶解症病例和一例戈勒姆病和斯托特病病例。骨质溶解症的发病机制尚不清楚，尚未发现能阻止其进展的治疗方法。
