| Literature DB >> 34813967 |
Joel Mudri1, Jane Lock2, Omkar Phadke3, Kelly Rouster-Stevens3, H Joon Kim4, Jason H Peragallo5.
Abstract
We present the case of an 8-year-old girl with chronic recurrent multifocal osteomyelitis (CRMO) involving the orbit and facial bone and causing left optic neuropathy. She presented with intermittent left periorbital swelling and a history of CRMO diagnosed 5 years earlier. Her disease responded well to adalimumab; however, delayed presentation resulted in permanent unilateral optic nerve atrophy and reduced vision. Orbital inflammatory disease is a rare manifestation of CRMO, and early recognition of the disease and treatment may prevent irreversible vision loss. CrownEntities:
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Year: 2021 PMID: 34813967 PMCID: PMC8976710 DOI: 10.1016/j.jaapos.2021.09.003
Source DB: PubMed Journal: J AAPOS ISSN: 1091-8531 Impact factor: 1.220