| Literature DB >> 26225043 |
Ujjwal Gulati1, Sujata Mohanty2, Jitender Dabas2, Nidhee Chandra3.
Abstract
Vanishing bone disease (VBD) is a rare disease of unknown etiology which is characterised by progressive replacement of bony framework by proliferation of endothelial lined lymphatic vessels. It has been given numerous names like massive osteolysis, Gorham's disease, phantom bone disease, and progressive osteolysis. It has no age, sex or race predilection. It may involve single or multiple bones and spread of the disease does not respect the relevant joint as boundary. The first report of the disease was published around two decades back but the mysterious nature of its etiology and ideal management strategy has still not been completely unfolded. The disease may functionally or aesthetically effect the patient and also has the potential to be life threatening. The first case of VBD in maxillofacial region was reported by Romer in 1924, Handbuch der speziellen pathologischen Anatomie and histology, Springer, Berlin. Since then, there have been few case reports of the same in maxillofacial region. We present a review of cases of VBD in maxillofacial region reported in literature along with our experience of a case.Entities:
Keywords: Bone resorption; Gorham’s disease; Haemangiomatosis; Lymphatic proliferation; Massive osteolysis
Year: 2015 PMID: 26225043 PMCID: PMC4511901 DOI: 10.1007/s12663-015-0746-9
Source DB: PubMed Journal: J Maxillofac Oral Surg ISSN: 0972-8270