Orbital amelanotic melanoma in xeroderma pigmentosum: a rare association.

dc.contributor.authorRizvi, Syed Aren_US
dc.contributor.authorAmitava, Abadan Ken_US
dc.contributor.authorMehdi, Ghazalaen_US
dc.contributor.authorSharma, Rajeeven_US
dc.contributor.authorAlam, Mohammad Sen_US
dc.date.accessioned2008-09-20en_US
dc.date.accessioned2009-05-29T07:45:33Z
dc.date.available2008-09-20en_US
dc.date.available2009-05-29T07:45:33Z
dc.date.issued2008-09-20en_US
dc.description.abstractXeroderma pigmentosum (XP) is an autosomal recessive genetic disorder of DNA repair in which the body's normal ability to repair damage caused by ultraviolet light is deficient. This leads to a 1000-fold increased risk of cutaneous and ocular neoplasms. Ocular neoplasms occurring in XP in order of frequency are squamous cell carcinoma, basal cell carcinoma and melanoma. Malignant melanomas occur at an early age in patients with XP. We report a case of XP with massive orbital melanoma in an eight-year-old boy which is unique due to its amelanotic presentation confirmed histopathologically.en_US
dc.description.affiliationInstitute of Ophthalmology, Jawaharlal Nehru Medical College, Aligarh, UP, India. draliraza12@hotmail.comen_US
dc.identifier.citationRizvi SA, Amitava AK, Mehdi G, Sharma R, Alam MS. Orbital amelanotic melanoma in xeroderma pigmentosum: a rare association. Indian Journal of Ophthalmology. 2008 Sep-Oct; 56(5): 421-3en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/69709
dc.language.isoengen_US
dc.source.urihttps://www.ijo.inen_US
dc.subject.meshChilden_US
dc.subject.meshDiagnosis, Differentialen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMelanoma, Amelanotic --complicationsen_US
dc.subject.meshOphthalmologic Surgical Procedures --methodsen_US
dc.subject.meshOrbiten_US
dc.subject.meshSkin Neoplasms --complicationsen_US
dc.subject.meshXeroderma Pigmentosum --complicationsen_US
dc.titleOrbital amelanotic melanoma in xeroderma pigmentosum: a rare association.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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