scholarly journals Brachymetacarpia and Brachymetatarsia in Patients with Multiple Hereditary Exostosis

2020 ◽  
Vol 12 (4) ◽  
pp. 549
Author(s):  
Yong Jin Cho ◽  
Jun Young Lee ◽  
Won Gyun Lee ◽  
Sung Taek Jung
Keyword(s):  
Multiple Hereditary Exostosis

Effect of Distal Ulna Osteochondroma Excision and Distal Ulnar Tether Release on Forearm Deformity in Preadolescent Patients With Multiple Hereditary Exostosis

2020 ◽  
Vol 40 (3) ◽  
pp. e222-e226 ◽  
Author(s):  
Christopher Belyea ◽  
Nicholas Pulos ◽  
Marybeth Ezaki ◽  
Lindley Wall ◽  
Janith Mills ◽  
...  
Keyword(s):  
Distal Ulna ◽  
Multiple Hereditary Exostosis

Hand Involvement in Multiple Hereditary Exostosis

Hand Clinics ◽  
1990 ◽  
Vol 6 (4) ◽  
pp. 685-692
Author(s):  
Virchel E. Wood ◽  
Christopher Molitor ◽  
M. Kenneth Mudge
Keyword(s):  
Multiple Hereditary Exostosis ◽  
Hand Involvement

scholarly journals Spinal Exostosis in a Boy with Multiple Hereditary Exostoses

2013 ◽  
Vol 2013 ◽  
pp. 1-4
Author(s):  
Ali Al Kaissi ◽  
Rudolf Ganger ◽  
Klaus Klaushofer ◽  
Franz Grill
Keyword(s):  
Spinal Cord ◽  
Ct Scanning ◽  
Cord Compression ◽  
Neurological Deficits ◽  
Posterior Arch ◽  
Thoracic Vertebrae ◽  
Multiple Hereditary Exostoses ◽  
Multiple Hereditary Exostosis ◽  
Multiple Exostoses ◽  
Spine Radiograph

We report on a 13-year-old boy who presented with multiple hereditary exostosis and had development of back pain, associated with neurological deficits, and was found to have exostoses in the spinal canal. Spine radiograph showed a cauliflower-like abnormality of multiple exostoses of the posterior arch (pedicle) of the thoracic vertebrae (T3–5). Reformatted CT scanning revealed the simultaneous development of intra- and extraspinal osteochondromatosis of T3–5. The spinal cord was compressed by the intraspinal exostosis. Our patient was surgically treated for intraspinal exostoses and showed cessation of neurological deficits. We report what might be a rare association of spinal cord compression in a patient with multiple hereditary exostoses.

scholarly journals Differential Diagnosis of Cartilaginous Lesions of Bone

2020 ◽  
Vol 144 (1) ◽  
pp. 71-82 ◽  
Author(s):  
David Suster ◽  
Yin Pun Hung ◽  
G. Petur Nielsen
Keyword(s):  
Differential Diagnosis ◽  
Massachusetts General Hospital ◽  
Surgical Excision ◽  
Benign Tumors ◽  
Low Grade ◽  
Case Review ◽  
Multiple Hereditary Exostosis ◽  
Tumors Of Bone ◽  
Well Differentiated ◽  
Cartilaginous Tumors

Context.— Cartilaginous tumors represent one of the most common tumors of bone. Management of these tumors includes observation, curettage, and surgical excision or resection, depending on their locations and whether they are benign or malignant. They can be diagnostically challenging, particularly in small biopsies. In rare cases, benign tumors may undergo malignant transformation. Objective.— To review common cartilaginous tumors, including in patients with multiple hereditary exostosis, Ollier disease, and Maffucci syndrome, and to discuss problems in the interpretation of well-differentiated cartilaginous neoplasms of bone. Additionally, the concept of atypical cartilaginous tumor/chondrosarcoma grade 1 will be discussed and its use clarified. Data Sources.— PubMed (US National Library of Medicine, Bethesda, Maryland) literature review, case review of archival cases at the Massachusetts General Hospital, and personal experience of the authors. Conclusions.— This review has examined primary well-differentiated cartilaginous lesions of bone, including their differential diagnosis and approach to management. Because of the frequent overlap in histologic features, particularly between low-grade chondrosarcoma and enchondroma, evaluation of well-differentiated cartilaginous lesions should be undertaken in conjunction with thorough review of the imaging studies.

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