Diffuse lymphangiomatosis of bone
Identifieur interne : 005A25 ( Istex/Curation ); précédent : 005A24; suivant : 005A26Diffuse lymphangiomatosis of bone
Auteurs : Daniel D. Maki ; Mark E. Nesbit ; Harry J. Griffiths [États-Unis]Source :
- Australasian Radiology [ 0004-8461 ] ; 1999-11.
Abstract
Two cases of lymphangiomatosis of bone, a very rare systemic condition characterized by both skeletal and parenchymal lesions, are presented. The skeletal changes have an appearance similar to haemangiomas in the spine, and soap‐bubbly lesions in the flat bones. One case carried the diagnosis of eosinophilic granuloma for 18 years. The findings on MRI, which have not been previously well‐established, are discussed.
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DOI: 10.1046/j.1440-1673.1999.00726.x
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Daniel D. Maki<affiliation><mods:affiliation>Department of Radiology, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania,,</mods:affiliation><wicri:noCountry code="subField"></wicri:noCountry></affiliation><affiliation><mods:affiliation>Department of Pediatric Oncology, University of Minnesota Medical School, Minneapolis, Minnesota and,</mods:affiliation><wicri:noCountry code="subField"></wicri:noCountry></affiliation>Le document en format XML
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