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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
1994-12-8
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pubmed:abstractText |
Gorham syndrome, also known as massive osteolysis or vanishing bone, is a rare disorder (135 cases reported) leading to extensive loss of bony matrix, replaced by proliferating thin-walled vascular channels. Three histologically proven cases of the disease are reported, including the clinical presentation and modern imaging features with CT (with 3D reconstruction) as well as T1- and T2-weighted MRI. Two cases in young women were located in the pelvis with extensive osteolysis reaching to the acetabulum. The third case in a 2-month-old boy is the youngest case ever reported and involved the humerus. The radiological appearance of the disease is discussed and the importance of the modern imaging methods debated.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0363-8715
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
18
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
985-9
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pubmed:dateRevised |
2005-11-16
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pubmed:meshHeading |
pubmed-meshheading:7962815-Acetabulum,
pubmed-meshheading:7962815-Adult,
pubmed-meshheading:7962815-Female,
pubmed-meshheading:7962815-Femur Head,
pubmed-meshheading:7962815-Follow-Up Studies,
pubmed-meshheading:7962815-Humans,
pubmed-meshheading:7962815-Humerus,
pubmed-meshheading:7962815-Infant,
pubmed-meshheading:7962815-Ischium,
pubmed-meshheading:7962815-Magnetic Resonance Imaging,
pubmed-meshheading:7962815-Male,
pubmed-meshheading:7962815-Middle Aged,
pubmed-meshheading:7962815-Osteolysis, Essential,
pubmed-meshheading:7962815-Pelvic Bones,
pubmed-meshheading:7962815-Pubic Bone,
pubmed-meshheading:7962815-Radiographic Image Enhancement,
pubmed-meshheading:7962815-Shoulder Fractures,
pubmed-meshheading:7962815-Tomography, X-Ray Computed
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pubmed:articleTitle |
CT and MRI of Gorham syndrome.
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pubmed:affiliation |
Radiologische Universitätsklinik Freiburg, Abteilung Röntgendiagnostik, Germany.
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pubmed:publicationType |
Journal Article,
Review,
Case Reports
|