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1.
J Bone Joint Surg Br ; 90(1): 61-5, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18160501

ABSTRACT

Antegrade intramedullary nailing of fractures of the shaft of the humerus is reported to cause impairment of the shoulder joint. We have reviewed 33 patients with such fractures to assess how many had injuries to the ipsilateral shoulder. All had an MR scan of the shoulder within 11 days of injury. The unaffected shoulder was also scanned as a control. There was evidence of abnormality in 21 of the shoulders (63.6%) on the injured side; ten had bursitis of the subacromial space, five evidence of a partial tear of the rotator cuff, one a complete rupture of the supraspinatus tendon, four inflammatory changes in the acromioclavicular joint and one a fracture of the coracoid process. These injuries may contribute to pain and dysfunction of the shoulder following treatment, and their presence indicates that antegrade nailing is only partly, if at all, responsible for these symptoms.


Subject(s)
Fracture Fixation, Intramedullary/adverse effects , Fractures, Bone/surgery , Humerus , Shoulder Injuries , Adult , Diaphyses/injuries , Diaphyses/surgery , Humans , Humerus/injuries , Humerus/surgery , Magnetic Resonance Imaging , Middle Aged
2.
J Bone Joint Surg Br ; 83(2): 269-72, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11284579

ABSTRACT

A five-day-old boy was referred with a soft-tissue mass in his right upper arm. Plain radiographs and ultrasound demonstrated a lesion extending from the axilla to the elbow on the posterolateral aspect of the humerus. Open biopsy confirmed the diagnosis of congenital haemangiopericytoma. After MRI and selective angiography, excision biopsy was carried out, but no adjuvant therapy was administered. At further examination, four years and ten months later, he was noted to have three small nodules at the site of the original tumour. Excision biopsy confirmed this to be a local recurrence, although the lesion was less cellular with no appreciable mitotic activity. Congenital haemangiopericytoma is a rare cause of a soft-tissue mass in children. Most tumours are benign, and recurrence is uncommon. The treatment is controversial, but most centres recommend the use of adjuvant chemotherapy, combined with complete excision. We recommend treatment with doxorubicin. Orthopaedic surgeons should be familiar with this tumour since 30% to 50% of cases occur in the limbs.


Subject(s)
Hemangiopericytoma/congenital , Soft Tissue Neoplasms/congenital , Arm , Chemotherapy, Adjuvant , Combined Modality Therapy , Hemangiopericytoma/therapy , Humans , Infant, Newborn , Male , Neoplasm Recurrence, Local , Soft Tissue Neoplasms/therapy
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