Publication:
Xeroderma pigmentosa – A disfiguring disease

creativeworkseries.issn1812-2027
dc.contributor.authorDW, Eugene
dc.contributor.authorKD, Joshi
dc.date.accessioned2025-07-21T09:00:44Z
dc.date.available2025-07-21T09:00:44Z
dc.date.issued2006
dc.description.abstractXeroderma pigmentosa is a rare inherited autosomal recessive disease with the inability to repair DNA damage caused by UV light. Recognized in the late 1800 by Maritz Kaposi it has been reported world wide and in al1 races with an over prevalence of 1-4 per million population. Kunwar et all 1,2. Those affected are extremely sensitive to the UV portion of the light and have a 2000 fold increased risk of skin cancer in the sun exposed skin. Basal cell carcinoma is the most commonly associated carcinoma followed by Squamous cell carcinoma and Melanoma. The pigmentation on the face and the rest of the body can be horribly disfiguring. The recurring cancer occurring on the face and repeated surgical treatment for the ulcerations have important social and psychological implications not encountered with other cancers3. We report two cases of BCC and melanoma. The first case is of BCC of the face in a teenaged girl coexisting with xeroderma pigmentosa. The second case presented with melanoma of the scalp in a 10years old female child. The details of these cases are presented and the management. Key Words: Xeroderma pigmentosa, Autosomal recessive, Basal cell carcinoma, Squamous cell carcinoma, Melanoma.
dc.identifier.urihttps://hdl.handle.net/20.500.14572/491
dc.language.isoen_US
dc.publisherKathmandu University
dc.titleXeroderma pigmentosa – A disfiguring disease
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage81
oaire.citation.startPage78
relation.isJournalIssueOfPublication77922bcd-b56e-4613-ac0d-25fdafc83480
relation.isJournalIssueOfPublication.latestForDiscovery77922bcd-b56e-4613-ac0d-25fdafc83480
relation.isJournalOfPublicationa782b7ff-cf89-4178-ad1c-11ed89cfe1bd

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