2019
DOI: 10.1111/ped.13938
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A case of Kawasaki disease complicated with retinal vasculitis

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Cited by 4 publications
(3 citation statements)
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“…The fundal findings in KD have not been fully examined in the currently available English literature, probably because of technical problems with examining infants/young children (usually younger than MIS-C patients). Posterior involvement in KD is rare and is usually limited to case reports ( 13 ). Similarly, fundus findings in MIS-C are scarce in the literature, but some reports have demonstrated normal findings, as described in this case ( 6 , 7 , 9 ).…”
Section: Discussionmentioning
confidence: 99%
“…The fundal findings in KD have not been fully examined in the currently available English literature, probably because of technical problems with examining infants/young children (usually younger than MIS-C patients). Posterior involvement in KD is rare and is usually limited to case reports ( 13 ). Similarly, fundus findings in MIS-C are scarce in the literature, but some reports have demonstrated normal findings, as described in this case ( 6 , 7 , 9 ).…”
Section: Discussionmentioning
confidence: 99%
“…Besides IVIG, she was treated with eye steroids and had total recovery within one month [ 7 ]. More recently, Suganuma et al described a seven-year-old boy who developed retinal vasculitis with impairment of visual acuity, and also refer to the only three reports in the literature with long-term visual impairment due to KD [ 8 ].…”
Section: Discussionmentioning
confidence: 99%
“…There are a few case reports of ophthalmic complications of KD, including retinitis, uveitis, and keratitis [8,14,15]. In one case report, photophobia and blurred vision developed three weeks after KD and was diagnosed as crystalline-like keratopathy and interpreted as a complication of IVIG administration [16].…”
Section: Ophthalmic Complicationsmentioning
confidence: 99%