| SCCH | sternocostoclavicular hyperostosis |
|---|---|
| SCCHO | sternocostoclavicular hyperostosis |
| VAH | vertebral ankylosing hyperostosis; Veterans Affairs Hospital; virilizing adrenal hyperplasia |
| hyperostosis frontalis interna | <radiology> Overgrowth of bone at the inner table of the frontal bone, usually bilateral and symmetrical, chiefly in females greater than 35 y.o., no clinical siginificance, unknown aetiology, irregular cortical thickening of the frontal area, spares areas occupied by superior sagital sinus and venous channels, may be 1 cm or thicker, occasionaly extends to parietal bones and orbital roofs, hyperostosis calvariae diffusa: variant of HFI: more diffuse thickening of vault (involving both tables) see: increased skull thickness (12 Dec 1998) |
|---|---|
| hyperostosis, sternocostoclavicular | A rare, benign rheumatologic disorder or syndrome characterised by hyperostosis and soft tissue ossification between the clavicles and the anterior part of the upper ribs. It is often associated with the dermatologic disorder palmoplantar pustulosis, particularly in japan. Careful diagnosis is required to distinguish it from psoriatic arthritis, osteitis deformans, and other diseases. Spondylitis of pustulosis palmaris et plantaris is one of the possible causes; also, evidence suggests one origin may be bone infection. Bone imaging is especially useful for diagnosis. It was originally described by sonozaki in 1974. (12 Dec 1998) |
| diffuse idiopathic skeletal hyperostosis | A form of degenerative arthritis characteristically associated with flowing calcification along the sides of the vertebrae of the spine and commonly with inflammation (tendinitis) and calcification of the tendons at their attachments points to bone. Because areas of the spine and tendons can become inflamed, antiinflammatory medications (NSAIDs), such ibuprofen, can be helpful in both relieving pain and inflammation. Also called Forestier's disease. (12 Dec 1998) |
| infantile cortical hyperostosis | Neonatal subperiosteal bone formation over many bones, especially the mandible and clavicles and the shafts of long bones; it follows fever, usually appearing before 6 months of age and disappearing during childhood. Synonym: Caffey's disease, Caffey's syndrome, Caffey-Silverman syndrome. (05 Mar 2000) |
| flowing hyperostosis | A hypertrophying and condensing osteitis which tends to run in longitudinal streaks or columns, like wax drippings on a candle, and which involves a number of the long bones. Synonym: flowing hyperostosis, streak hyperostosis. Origin: rheo-+ G. Osteon, bone, + -osis, condition (05 Mar 2000) |