Xeroderma pigmentosum with ocular involvement and squamous cell carcinoma: A case report

Bernadya Yogatri Anjuwita Saputri, Iskandar Zulkarnain

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)


Xeroderma Pigmentosum is a rare, autosomal recessive genetic disorder, characterized by defective DNA repair leading to clinical and cellular hypersensitivity to ultraviolet radiation and carcinogenic agents. Patients with xeroderma pigmentosum often have cutaneous and ocular sun sensitivity and freckle-like skin pigmentation. Skin changes are the most important symptoms and they manifest as erythema, painful blisters and ulceration. The last level of skin changes transformation are malignant neoplasms, particularly squamous cell carcinoma. There is a great involvement of many parts of the body, especially the head and neck. This paper describes a case of xeroderma pigmentosum with advanced cutaneous squamous cell carcinoma and ocular lesions in a nine-year-old boy. The extensive ultraviolet radiation-induced skin and eye damage are evidence of a failure to use sun-protection and a lack of appropriate medical care from childhood.

Original languageEnglish
Pages (from-to)153-156
Number of pages4
JournalDermatology Reports
Issue numberS1
Publication statusPublished - 2019


  • Genetic skin disorder
  • Pigmentary retinal degeneration
  • Squamous cell carcinoma
  • Xeroderma pigmentosum


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