1. CT and MRI of Gorham Syndrome
- Author
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G. Sigmund, B. Stöver, Hauenstein Kh, C. P. Adler, M O Tanyü, and P. Vinee
- Subjects
Adult ,Male ,medicine.medical_specialty ,Osteolysis ,Ischium ,medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Femur ,Humerus ,Pelvic Bones ,Pelvis ,Pubic Bone ,medicine.diagnostic_test ,business.industry ,Infant ,Acetabulum ,Femur Head ,Magnetic resonance imaging ,Anatomy ,Middle Aged ,medicine.disease ,Magnetic Resonance Imaging ,Radiographic Image Enhancement ,medicine.anatomical_structure ,Shoulder Fractures ,Vascular channel ,Female ,Osteolysis, Essential ,Radiology ,Presentation (obstetrics) ,Tomography, X-Ray Computed ,business ,Follow-Up Studies - Abstract
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.
- Published
- 1994
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