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- W2087626709 abstract "Gorham disease is a rare bone disorder characterized by osteolysis, angiomatous proliferation, and soft-tissue swelling with absence of new bone formation. Although the first case was reported by Jackson in 1838, 1 Jackson J.B.S. A boneless arm. Boston Med Surg J. 1838; 18: 368-369 Crossref Google Scholar it was not until 1955 when Gorham and Stout established the clinical and pathological features. 2 Gorham L.W. Stout A.P. Massive osteolysis (acute spontaneous absorption of bone, phantom bone, disappearing bone): its relation to haemangiomatosis. J Bone Joint Surg Am. 1955; 37: 985-1004 PubMed Google Scholar , 3 Chung C. Yu J.S. Resnick D. et al. Gorham syndrome of the thorax and cervical spine: CT and MRI findings. Skeletal Radiol. 1997; 26: 55-59 Crossref PubMed Scopus (28) Google Scholar , 4 Vinee P. Tanyu M.O. Hauenstein K.H. et al. CT and MRI of Gorham syndrome. J Comput Assist Tomogr. 1994; 18: 985-989 Crossref PubMed Scopus (51) Google Scholar The disease is extremely rare with approximately 175 cases reported in the literature. 5 Moller G. Priemel M. Amling M. et al. The Gorham-Stout syndrome (Gorham's massive osteolysis). J Bone Joint Surg Br. 1999; 81-B: 501-506 Crossref Scopus (136) Google Scholar In this report, we present three pathologically proven cases of Gorham disease and a review of the imaging findings." @default.
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- W2087626709 date "2006-12-01" @default.
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- W2087626709 title "Gorham disease of bone: three cases and review of radiological features" @default.
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- W2087626709 doi "https://doi.org/10.1016/j.crad.2006.04.014" @default.
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