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1.
J Orthop Trauma ; 36(9): 481-488, 2022 09 01.
Article de Anglais | MEDLINE | ID: mdl-35171136

RÉSUMÉ

LEVEL OF EVIDENCE: Therapeutic Level V. See Instructions for Authors for a complete description of levels of evidence.

2.
J Knee Surg ; 35(6): 597-606, 2022 May.
Article de Anglais | MEDLINE | ID: mdl-35189664

RÉSUMÉ

Intra-articular tumors of the knee are most commonly benign. Overall, this is a relatively rare clinical presentation. The differential diagnosis includes pigmented villonodular synovitis, synovial chondromatosis, lipoma arborescens, synovial hemangioma, and very rarely primary sarcoma (synovial sarcoma being the most common). The clinical presentation for these conditions is usually non-specific, but radiographic and advanced imaging findings are able to differentiate some of these tumors. It is essential to obtain and send tissue specimens to pathology for histologic analysis to rule out a primary malignancy as a missed diagnosis can have grave implications on patient outcomes. This review summarized key aspects of diagnosis and treatment for these conditions.


Sujet(s)
Chondromatose synoviale , Lipome , Synovite villonodulaire pigmentaire , Chondromatose synoviale/diagnostic , Chondromatose synoviale/anatomopathologie , Humains , Genou/anatomopathologie , Articulation du genou/imagerie diagnostique , Articulation du genou/anatomopathologie , Articulation du genou/chirurgie , Lipome/diagnostic , Lipome/chirurgie , Imagerie par résonance magnétique , Synovite villonodulaire pigmentaire/diagnostic , Synovite villonodulaire pigmentaire/chirurgie
3.
J Knee Surg ; 35(6): 585-596, 2022 May.
Article de Anglais | MEDLINE | ID: mdl-35181876

RÉSUMÉ

Primary bone sarcomas and aggressive benign bone tumors are relatively rare. It is essential to recognize features that are concerning for these aggressive tumors based on a patient's history, physical exam, and radiographs. Physicians and other health care providers should have a high suspicion for these tumors and promptly refer these patients to orthopaedic oncologists. A multidisciplinary, team-based approach is required to obtain an accurate diagnosis and provide comprehensive care. This review discussed the appropriate work-up, biopsy principles, relevant peri-operative medical management, and surgical treatment options for patients with aggressive primary bone tumors around the knee. Primary bone sarcomas (osteosarcoma and chondrosarcoma) and aggressive benign bone tumors (giant cell tumor, chondroblastoma, and chondromyxoid fibroma) that have a predilection to the distal femur and proximal tibia are the focus of this review.


Sujet(s)
Tumeurs osseuses , Chondroblastome , Chondrosarcome , Ostéosarcome , Tumeurs des tissus mous , Tumeurs osseuses/diagnostic , Tumeurs osseuses/chirurgie , Chondroblastome/diagnostic , Chondroblastome/anatomopathologie , Chondroblastome/chirurgie , Chondrosarcome/chirurgie , Humains , Genou/anatomopathologie , Ostéosarcome/chirurgie
4.
J Knee Surg ; 35(6): 619-624, 2022 May.
Article de Anglais | MEDLINE | ID: mdl-35181877

RÉSUMÉ

Metastatic disease affecting the proximal tibia is rarer than disease affecting the femur; however, it presents unique challenges that the orthopaedic surgeon must address to ensure successful outcomes and return the patient to an ambulatory status. The essential workup for evaluating and treating these patients is addressed briefly in this review as a summary of the information is provided in part 1 of this series. Part 2 of this series will focus on the surgical treatment of these lesions, which can be complex and is not as well described in the literature. Procedures ranging from open reduction internal fixation with cement augmentation to complex endoprosthetic reconstruction can be employed to address proximal tibia metastatic disease. An awareness of these various treatment modalities allows the orthopaedic surgeon to plan the most effective operation for the patients under their care.


Sujet(s)
Fractures spontanées , , Fémur/chirurgie , Humains , Articulation du genou/chirurgie , Études rétrospectives , Tibia/chirurgie , Résultat thérapeutique
5.
Skeletal Radiol ; 40(7): 943-6, 2011 Jul.
Article de Anglais | MEDLINE | ID: mdl-21499979

RÉSUMÉ

Parachordoma is a rare tumor, with fewer than 100 cases reported. We present an unusual presentation of a long tumor tracking along the median nerve, with regional metastasis to the axillary nodes in a 67-year-old woman. The tumor extended from the wrist proximally along the forearm to the elbow, coursing intraneurally along the median nerve. We present this case due its rarity, interesting radiographic appearance, and atypical presentation.


Sujet(s)
Bras/anatomopathologie , Chordome/anatomopathologie , Chordome/secondaire , IRM dynamique/méthodes , Tumeurs des tissus mous/anatomopathologie , Tumeurs des tissus mous/secondaire , Sujet âgé , Femelle , Humains
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