Unravelling the unique case of congenital infiltrating lipomatosis of face with its rare associations—A case report
Journal of Oral Biology and Craniofacial Research, ISSN: 2212-4268, Vol: 14, Issue: 6, Page: 767-772
2024
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
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Article Description
Congenital infiltrating lipomatosis of facial (CIL-F) is a rare tumour of adipose tissue resulting in a progressive craniofacial deformity with involvement of the underlying bones, muscles and joints. We report a very rare case of CIL-F with left sided temporomandibular joint ankylosis in a young patient who presented with facial swelling and reduced mouth opening. This case highlights the imaging features, differential diagnosis and brief management of CIL-F with special emphasis on CT and MRI findings. Also, some associations of CIL-F such as TMJ ankylosis and extraocular muscle hypertrophy has been described, which has been reported very rarely.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2212426824001532; http://dx.doi.org/10.1016/j.jobcr.2024.10.006; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85206621515&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/39497910; https://linkinghub.elsevier.com/retrieve/pii/S2212426824001532; https://dx.doi.org/10.1016/j.jobcr.2024.10.006
Elsevier BV
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