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  • 1
    Online Resource
    Online Resource
    S. Karger AG ; 2018
    In:  Ocular Oncology and Pathology Vol. 4, No. 3 ( 2018), p. 182-185
    In: Ocular Oncology and Pathology, S. Karger AG, Vol. 4, No. 3 ( 2018), p. 182-185
    Abstract: 〈 b 〉 〈 i 〉 Background: 〈 /i 〉 〈 /b 〉 There are several cysts that can occur in the iris. The midzonal (retroiridic) iris pigment epithelial (IPE) cyst is important because it can simulate melanoma of the ciliary body. However, it is frequently asymptomatic and requires no treatment. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 A 37-year-old asymptomatic woman with visual acuity of 20/20 in each eye was found to have an elevated mass behind the left iris, presumed to be melanoma, and was referred for management. On our examination, there was a typical midzonal IPE cyst in the left eye (OS), requiring observation without intervention. After 4 years, she developed progressive visual loss to 20/40 OS and cyst enlargement was noted, obstructing most of the visual axis and causing partial lens subluxation. Translimbal fine needle aspiration deflation with a 30-G needle was performed. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 Immediately at aspiration, the cyst demonstrated collapse, disappearing behind the iris stroma, and the lens subluxation resolved. Visual acuity returned to 20/20 OS and has remained stable without recurrence for 3 years. 〈 b 〉 〈 i 〉 Conclusion: 〈 /i 〉 〈 /b 〉 Although most midzonal IPE cysts are asymptomatic, this case showed progressive enlargement with visual loss and was managed with translimbal aspiration. Symptomatic midzonal IPE cysts can be deflated with translimbal aspiration rather than more aggressive surgical excision.
    Type of Medium: Online Resource
    ISSN: 2296-4681 , 2296-4657
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2018
    detail.hit.zdb_id: 2806965-1
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  • 2
    Online Resource
    Online Resource
    SLACK, Inc. ; 2014
    In:  Journal of Pediatric Ophthalmology & Strabismus Vol. 51, No. 6 ( 2014-11)
    In: Journal of Pediatric Ophthalmology & Strabismus, SLACK, Inc., Vol. 51, No. 6 ( 2014-11)
    Abstract: A child referred for management of retinoblastoma who alternatively had a calcified scleral choristoma as part of previously undiagnosed organoid nevus syndrome is described. A 31-month-old male infant with scalp alopecia was referred for retinoblastoma management after a calcified mass in his left eye was found. Ophthalmic examination revealed the mass was of choroidal or scleral origin, underlying the retina. The amelanotic circumpapillary mass extended superonasally in a geographic configuration and measured 14 × 12 mm. There was no subretinal fluid, hemorrhage, feeder vessels, or tumor seeding. Ocular ultrasonography confirmed a homogeneous calcified intraocular mass 3.1 mm in thickness. Enhanced depth imaging optical coherence tomography revealed that the lesion was located within the sclera compressing the overlying choroidal tissue. Further evaluation disclosed cutaneous aplasia cutis congenita with nevus sebaceous of Jadassohn. Magnetic resonance imaging disclosed an arachnoid cyst of the brain. Later, optical coherence tomography revealed the mass to be in the deep choroid or within the sclera. This constellation of ocular, cutaneous, and neurological features were suggestive of organoid nevus syndrome. At the 2-year follow-up, the findings were stable. The calcified choristoma of organoid nevus syndrome, located within the sclera in this case, has distinctive clinical features that differentiate this benign tumor from retinoblastoma. [J Pediatr Ophthalmol Strabismus 2014;51:e1–e3.]
    Type of Medium: Online Resource
    ISSN: 0191-3913 , 1938-2405
    Language: English
    Publisher: SLACK, Inc.
    Publication Date: 2014
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