A case of lip squamous cell carcinoma with a familial history of Xeroderma pigmentosum

Oral Oncol. 2020 Dec:111:104896. doi: 10.1016/j.oraloncology.2020.104896. Epub 2020 Jul 10.

Abstract

Xeroderma pigmentosum is an orphan hereditary photosensitive human disorder that is recognized by the development of skin lesions in sun-exposed regions of the body due to severe photosensitivity. Patients with this condition have an abnormal DNA repair process due to a genetic mutation. Xeroderma pigmentosum is considered as a risk factor of cancer since the affected population may develop various cutaneous cancers including both melanoma and non-melanoma cutaneous malignancies even at a younger age than the general population. This risk concerns also asymptomatic heterozygote individuals. Here, we present a case of 46 years old man with a familial history of Xeroderma pigmentosum who developed a microscopically confirmed squamous cell carcinoma of the lip.

Keywords: Familial history; Lip squamous cell carcinoma; Microscopic surgery; Reconstruction; Xeroderma pigmentosum.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Carcinoma, Squamous Cell / pathology*
  • Carcinoma, Squamous Cell / surgery
  • Humans
  • Lip Neoplasms / pathology*
  • Lip Neoplasms / surgery
  • Lymph Nodes / pathology
  • Male
  • Middle Aged
  • Neck
  • Xeroderma Pigmentosum / complications*
  • Xeroderma Pigmentosum / genetics