Literature DB >> 19516012

A quantitative assessment of the burden and distribution of Lisch nodules in adults with neurofibromatosis type 1.

Sean Boley1, Jennifer L Sloan, Alexander Pemov, Douglas R Stewart.   

Abstract

PURPOSE: The presence of two or more Lisch nodules (melanocytic hamartomas of the iris) is one of seven diagnostic criteria for neurofibromatosis type 1 (NF1), a common monogenic disorder of dysregulated neurocutaneous growth. The hypothesis that Lisch nodules arise secondary to exposure to ultraviolet (UV) radiation from sunlight was investigated.
METHODS: Lisch nodule burden was mapped and quantified in the irides of 77 adults with NF1. Lifetime sunlight (UV radiation) exposure was inventoried, NF1 neurocutaneous severity determined, and two NF1 mutations predictive of severity selectively genotyped.
RESULTS: There was high interindividual variability in Lisch nodule burden. Lisch nodules were primarily located in the inferior hemifield (half) of the iris, regardless of its color (P = 3.0 x 10(-20)). Light irides harbored significantly more Lisch nodules than dark irides (P = 4.8 x 10(-5)). There was no statistically significant correlation of Lisch nodule burden to lifetime sunlight exposure "dose" or NF1 neurocutaneous severity.
CONCLUSIONS: The difference in Lisch nodule burden between the superior and inferior iris hemifields is most likely due to the sunlight-shielding effects on the superior half by periocular structures. The difference in Lisch nodule burden between light and dark irides is probably due to the photoprotective effects of pigmentation. The genes underlying the control of iris color may thus be viewed as modifiers of severity of Lisch nodule burden in NF1. Given the role of UV radiation and, presumably, DNA damage in Lisch nodule pathogenesis, "benign tumor of the iris," not "hamartoma," may be a better descriptor.

Entities:  

Mesh:

Year:  2009        PMID: 19516012      PMCID: PMC2883270          DOI: 10.1167/iovs.09-3650

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  43 in total

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Authors:  Bradley T Smith; Shaleen Belani; Allen C Ho
Journal:  Int Ophthalmol Clin       Date:  2005

2.  Inferior predilection of Lisch nodules with ptosis.

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Journal:  Neurology       Date:  2005-04-26       Impact factor: 9.910

3.  A novel sensor array for field based ocular ultraviolet radiation measurements.

Authors:  D P Fleming; J E Walsh; L A Moore; J P Bergmanson; D McMahon
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4.  Inferior predilection of Lisch nodules with ptosis.

Authors:  David T L Liu; Alice Y K Chan; Paul C L Cho
Journal:  Neurology       Date:  2006-02-28       Impact factor: 9.910

5.  Mitotic recombination as evidence of alternative pathogenesis of gastrointestinal stromal tumours in neurofibromatosis type 1.

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7.  Ultraviolet light exposure as a risk factor for ocular melanoma in Queensland, Australia.

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Review 9.  Role of ocular melanin in ophthalmic physiology and pathology.

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3.  Left-right asymmetry in a case of bilateral Lisch nodules.

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Review 4.  Ophthalmological assessment of children with neurofibromatosis type 1.

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5.  Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis.

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6.  Predictive Modeling for Clinical Features Associated With Neurofibromatosis Type 1.

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Review 7.  Challenges in the diagnosis of neurofibromatosis type 1 (NF1) in young children facilitated by means of revised diagnostic criteria including genetic testing for pathogenic NF1 gene variants.

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