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Osteochondromatosis of the Shoulder in a Twelve-Year-Old Boy : Case Report Hiroyuki Katoh 1 , Kiyohisa Ogawa 1 , Hiroyasu Ikegami 1 , Wataru Inokuchi 1 , Yoshiaki Toyama 1 1Department of Orthopaedic Surgery, School of Medicine, Keio University Keyword: osteochondromatosis , 骨軟骨腫症 , osteochondritis dissecans , 離断性骨軟骨炎 , shoulder joint , 肩関節 pp.101-104
Published Date 2004/1/1
DOI https://doi.org/10.11477/mf.1408100359
  • Abstract
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 We present a rare case of secondary osteochondromatosis in the shoulder joint of a twelve-year-old boy, and discuss the possible etiology of the condition. In December 1999, a twelve-year-old boy presented with pain in the right shoulder after conducting a back flip a month earlier. Radiographs revealed multiple calcified bodies in the shoulder joint and the axillary area. MRI revealed severe synovitis and an edematous lesion in the medial humeral head. An arthroscopic extraction of the calcified bodies was performed and histological examination of the extracted bodies led to the diagnosis of secondary osteochondromatosis. Of the numerous conditions that may lead to secondary osteochondromatosis, osteochondritis dissecans may have been the precipitating condition in this case. Two years after surgery, the patient has no complaints of pain, and there are no remarkable findings upon physical examination. MRI revealed that an irregularity in the subchondral bone and a chondral depression remained in the medial humeral head. There have been no recurrences of free bodies during the two year follow-up period.


Copyright © 2004, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1286 印刷版ISSN 0557-0433 医学書院

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