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International Journal of Oral Surgery, 1983
This report describes a rare case of restricted mandibular opening caused by zygomatic exostosis and hyperplasia of the coronoid process. Computed tomography revealed the presence of a pseudojoint between the exostosis and the enlarged coronoid process; the bony restriction was surgically removed through an intraoral approach. Only 3 similar cases have
T, Boland, O, Ross Beirne
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This report describes a rare case of restricted mandibular opening caused by zygomatic exostosis and hyperplasia of the coronoid process. Computed tomography revealed the presence of a pseudojoint between the exostosis and the enlarged coronoid process; the bony restriction was surgically removed through an intraoral approach. Only 3 similar cases have
T, Boland, O, Ross Beirne
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The Journal of Foot and Ankle Surgery, 1995
The author describes subungual exostoses as well as their differential diagnoses. Clinical and radiologic features are illustrated. Surgical excision is recommended, following partial toenail avulsion, in the majority of symptomatic cases.
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The author describes subungual exostoses as well as their differential diagnoses. Clinical and radiologic features are illustrated. Surgical excision is recommended, following partial toenail avulsion, in the majority of symptomatic cases.
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Dupuytrenʼs (Subungual) Exostosis
The American Journal of Surgical Pathology, 1988Because it may produce a bewildering array of histologic patterns, the clinical entity of subungual exostosis (Dupuytren's exostosis), is sometimes confused with chondrosarcoma. However, this lesion is a distinct entity. It begins as a reactive growth of cellular fibrous tissue and metaplastic cartilage, which undergoes enchondral ossification.
A, Miller-Breslow, H D, Dorfman
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Subungual (Dupuytrenʼs) Exostosis
Journal of Pediatric Orthopaedics, 1995Dupuytren's subungual exostosis is an uncommon osteochondral lesion affecting the distal phalanx of adolescents. Lack of awareness of this unusual lesion causes many to be initially misdiagnosed. Accurate diagnosis based on clinical findings and radiographs and appropriate treatment methods are outlined.
H, Multhopp-Stephens, A K, Walling
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The Journal of Bone and Joint Surgery. British volume, 1963
1. Hereditary multiple exostosis has been studied in fifty-six patients and their relatives. In most cases previous records were available and the progress of the disease could be traced over many years. 2. The characteristic lesions are described and the complications encountered in the present series of cases are noted.
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1. Hereditary multiple exostosis has been studied in fifty-six patients and their relatives. In most cases previous records were available and the progress of the disease could be traced over many years. 2. The characteristic lesions are described and the complications encountered in the present series of cases are noted.
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