Choroidal ganglioneuromas in Francois variant neurofibromatosis-1: A rare retinoblastoma mimic

dc.contributor.authorGupta, Himikaen_US
dc.contributor.authorKandalkar, Bhuvaneshwarien_US
dc.date.accessioned2023-08-25T06:33:45Z
dc.date.available2023-08-25T06:33:45Z
dc.date.issued2022-07
dc.description.abstractNeurofibromtosis-1 (NF-1) is the commonest oculo-neuro-cutaneous syndrome with multiple ocular manifestations. Reporting three children who presented with unilateral glaucoma (buphthalmos), ipsilateral facial hemihypertrophy, and eyelid plexiform neurofibroma: completing the triad of François syndrome, a rare NF1 variant. Two presented with leukocoria and were referred to as retinoblastoma suspects. Histopathology showed ganglioneuroma, a benign choroidal tumor, associated with NF-1, which does not need treatment. Knowledge of this rare condition avoids misdiagnosis of retinoblastoma, prevents aggressive management, and the associated psychological impact.en_US
dc.identifier.affiliationsDepartment of Pediatric Ophthalmology and Pediatric Pathology, SRCC Children’s Hospital Managed by NH- Mumbai, Maharashtra, Indiaen_US
dc.identifier.citationGupta Himika, Kandalkar Bhuvaneshwari. Choroidal ganglioneuromas in Francois variant neurofibromatosis-1: A rare retinoblastoma mimic. Indian Journal of Ophthalmology. 2022 Jul; 70(7): 2602-2605en_US
dc.identifier.issn1998-3689
dc.identifier.issn0301-4738
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/224439
dc.languageenen_US
dc.publisherAll India Ophthalmological Societyen_US
dc.relation.issuenumber7en_US
dc.relation.volume70en_US
dc.source.urihttps://doi.org/10.4103/ijo.IJO_3109_21en_US
dc.subjectBuphthalmosen_US
dc.subjectFrançois syndromeen_US
dc.subjectneurofibromatosisen_US
dc.subjectretinoblastoma mimicen_US
dc.titleChoroidal ganglioneuromas in Francois variant neurofibromatosis-1: A rare retinoblastoma mimicen_US
dc.typeJournal Articleen_US
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