Gorham-Stout disease and generalized lymphatic anomaly—clinical, radiologic, and histologic differentiation-Reference-Cited by-同舟云学术

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Gorham-Stout disease and generalized lymphatic anomaly—clinical, radiologic, and histologic differentiation

Published:2013-01-31 Issue:7 Volume:42 Page:917-924
ISSN:0364-2348
Container-title:Skeletal Radiology
language:en
Short-container-title:Skeletal Radiol

Author:

Lala Shailee,Mulliken John B.,Alomari Ahmad I.,Fishman Steven J.,Kozakewich Harry P.,Chaudry Gulraiz

Publisher

Springer Science and Business Media LLC

Subject

Radiology Nuclear Medicine and imaging

Link

http://link.springer.com/content/pdf/10.1007/s00256-012-1565-4.pdf

Reference17 articles.

1. Jackson J. A boneless arm. Boston Med Surg J. 1838;18:368–9.

2. Gorham LW, Wright AW, Shultz HH, Maxon FC Jr. Disappearing bones: a rare form of massive osteolysis; report of two cases, one with autopsy findings. Am J Med. 1954;17(5):674–82.

3. Gorham LW, Stout AP. Massive osteolysis (acute spontaneous absorption of bone, phantom bone, disappearing bone); its relation to hemangiomatosis. J Bone Joint Surg Am. 1955;37-A:985–1004.

4. Bruch-Gerharz D, Gerharz CD, Stege H, et al. Cutaneous lymphatic malformations in disappearing bone (Gorham-Stout) disease: a novel clue to the pathogenesis of a rare syndrome. J Am Acad Dermatol. 2007;56:S21–5.

5. Hammer F, Kenn W, Wesselmann U, et al. Gorham-Stout disease–stabilization during bisphosphonate treatment. J Bone Miner Res. 2005;20:350–3.

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