Pigmented Xerodermoid.

Indian Pediatr

Department of Dermatology, Katihar Medical College, Bihar and #Department of Pediatrics, SMS Medical College, Jaipur, India.

Published: January 2016

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Xeroderma pigmentosum (XP) is a rare autosomal recessive disease; relatively mild XP patients are sometimes designated as having pigmented xerodermoid or xerodermoid pigmentosum (XP-V), a variant of XP. It is commonly associated with many long-standing skin conditions and tumors, including malignancies, management of which is necessary to prevent the progress of the disease. The objective of the study was to evaluate an innovative therapeutic treatment, beyond surgery, surgical excision, cryotherapy, electrocautery and curettage, or Mohs surgery, for the management of skin tumors in XP.

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Xeroderma pigmentosum (XP) is a rare autosomal recessive disease; relatively mild XP patients are sometimes designated as having pigmented xerodermoid or xerodermoid pigmentosum (XP-V), a variant of XP. It is commonly associated with many long-standing skin conditions and tumors, including malignancies, management of which is necessary to prevent the progress of the disease. The objective of the study was to report the use of a number of innovative therapeutic and prophylactic treatments, beyond surgery, such as topical 5-fluorouracil, topical imiquimod, other topical immunomodulators, or photodynamic therapy, in treating skin eruptions and their complications in XP patients.

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Pigmented Xerodermoid.

Indian Pediatr

January 2016

Department of Dermatology, Katihar Medical College, Bihar and #Department of Pediatrics, SMS Medical College, Jaipur, India.

View Article and Find Full Text PDF

Pigmented xerodermoid.

Indian J Dermatol Venereol Leprol

July 2007

Department of Skin and STD, Fr. Muller's Medical College, Kankanady, Mangalore-575 002, India.

An 18-year-old female who presented with features suggestive of pigmented xerodermoid is reported.

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Pigmented xerodermoid, a rare genodermatosis, presents with clinical features and pathology similar to xeroderma pigmentosum, but at a later age. DNA repair replication is normal, but there is total depression of DNA synthesis after exposure to UV radiation. Two siblings in their teens and a man in his thirties with features of pigmented xerodermoid, e.

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