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pro vyhledávání: '"PVNS - Pigmented villonodular synovitis"'
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Autor:
Navin Nayan, Vikas K Jagat
Publikováno v:
National Journal of Medical Research, Vol 6, Iss 02 (2016)
This is a case report of a 13 year old boy who has been operated for Pigmented Villonodular Synovitis (PVNS) and treated with adjuvant post-operative radiotherapy for incomplete surgical resection. This report mainly highlights the role of radiothera
Externí odkaz:
https://doaj.org/article/7e3f669a863a4139ae9d44dda9630e2c
Publikováno v:
International Journal of Orthopaedics Sciences. 5:311-313
Publikováno v:
Radiology Case Reports
We present a case report of a rare synovial hemangioma of the knee. Magnetic resonance imaging (MRI) demonstrated typical signal characteristics and enhancement. Histologic findings were confirmatory. Imaging characteristics, differential diagnoses a
Publikováno v:
RadioGraphics. 28:2069-2086
Publikováno v:
RadioGraphics. 28:1519-1523
Publikováno v:
Diagnostic Imaging of the Foot and Ankle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a36f34f5d15648f0f024b0a2ba0d297
https://doi.org/10.1055/b-0034-102497
https://doi.org/10.1055/b-0034-102497
Publikováno v:
Radiographics : a review publication of the Radiological Society of North America, Inc. 29(3)
A wide spectrum of entities may give rise to soft-tissue masses in children, including benign and malignant tumors, pseudotumors, and both neoplastic and nonneoplastic vascular lesions. Because of its excellent tissue contrast, multiplanar capability
Autor:
Benjamin Plotkin, Rajeev Varma
Publikováno v:
Radiology Case Reports
We present a case of lipoma arborescens of the knee in a 17-year-old man, discuss its characteristic imaging findings, and review the relevant differential diagnoses.
Publikováno v:
Radiology Case Reports
There are only a few reported cases in the literature of pigmented villonodular synovitis (PVNS) involving the elbow. Even more rare is its occurrence in the pediatric population as this condition mainly affects young adults. We report a unique case