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Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb)

open access: yesHuman Mutation, 2009
: Multiple osteochondromas (MO) is an autosomal dominant skeletal disease characterized by the formation of multiple cartilage-capped bone tumors growing outward from the metaphyses of long tubular bones.
Elena Pedrini   +2 more
exaly   +1 more source
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On spinal osteochondromas

Journal of Neurosurgery, 1992
✓ Osteochondromas (or osteocartilaginous exostoses) make up about 30% to 40% of benign bone tumors. Most are solitary lesions but some are multiple, usually with autosomal dominant inheritance. From 1% to 4% of osteochondromas occur in the spine, where they can cause a variety of signs and symptoms, including those of spinal cord or spinal root ...
S, Albrecht   +2 more
openaire   +2 more sources

Osteochondroma of the mandible

Oral Surgery, Oral Medicine, Oral Pathology, 1974
Abstract Cartilage-capped exostoses, although frequently seen in the general skeleton, occur only rarely in the mandible. Two additional mandibular cases are here added to the few previously reported. The majority of cases seem to represent either developmental anomalies or examples of reactive hyperplasia. True neoplasms are extremely rare.
J H, Allan, J, Scott
openaire   +2 more sources

Osteochondroma of the tongue

The Journal of Laryngology & Otology, 1990
AbstractA case is described of osteochondroma of the tongue and the literature on osteomata, chondromata and osteochondromata of the tongue is reviewed. The tendency for these tumours to arise in the region of the foramen caecum has been noted in previous reports as has the female preponderance.
C, Watson, J A, Crowther, M R, Stephen
openaire   +2 more sources

Subacromial Osteochondroma

Orthopedics, 2011
The most common cause of impingement syndrome is mechanical irritation of the subacromial bursa and rotator cuff by the coracoacromial arch. Offending structures include the undersurface of the anterolateral acromion, coracoacromial ligament, and the undersurface of the distal clavicle.
Michael T, Lu, Joseph A, Abboud
openaire   +2 more sources

Osteochondroma and Hereditary Multiple Osteochondromas

2021
Osteochondroma is the most common bone tumor, mainly affecting patients under 20 years of age. It presents in 90% of the cases as a solitary lesion. The remaining cases are part of the multiple hereditary osteochondromas syndrome. The pathogenesis is not entirely clear. Osteochondromas usually develop at the metaphysis of long bones.
openaire   +1 more source

The ?Disappearing? osteochondroma

Skeletal Radiology, 1983
Spontaneous regression of a solitary osteochondroma is described. This regression apparently resulted from a cessation of growth of the osteochondroma prior to skeletal maturation, with subsequent incorporation of the lesion into the enlarging bony metaphysis.
openaire   +2 more sources

Osteochondroma of the Clivus

Australasian Radiology, 1979
SUMMARYA case of an osteochondroma, arising from the base of the skull is reported and the literature is reviewed. In particular, computerized tomography proved extremely valuable in confirming the diagnosis, defining the extent of the tumour mass, and assessing the effect on adjacent brain tissue.
G, Fon, M R, Sage
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Recurrent osteochondroma

The Journal of Foot and Ankle Surgery, 1998
Osteochondroma is the most common bone tumor of the foot. This should be easily recognized by foot and ankle specialists. Malignant transformation does occur, although it is quite rare, and should be a consideration when deciding on treatment. An unusual case of recurrent osteochondroma is reviewed.
F N, Day, C, Ruggieri, C, Britton
openaire   +2 more sources

Osteochondromas of the spine

Clinical Radiology, 2014
Osteochondromas are common developmental benign bone lesions, which rarely involve the spine. In a narrow space, such as the spinal canal, they may potentially lead to serious complications. Moreover, because this condition is fairly rare in the spine, it may be confused with other entities.
A, Sinelnikov, H, Kale
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