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Case Reports
. 2010 Sep;33(7):495.e1-4.
doi: 10.1016/j.jfo.2010.06.001. Epub 2010 Jul 31.

[Xeroderma pigmentosum associated with intracerebral tumor: a case report]

[Article in French]
Affiliations
Case Reports

[Xeroderma pigmentosum associated with intracerebral tumor: a case report]

[Article in French]
K El Ouazzani Chahdi et al. J Fr Ophtalmol. 2010 Sep.

Abstract

Patients with the genetic disease xeroderma pigmentosum (XP) lack the ability to carry out a specific type of DNA repair process called nucleotide excision repair (NER). The NER pathway plays a critical role in the repair of DNA damage resulting from ultraviolet (UV) radiation. We report a case of a patient presenting a cutaneous form of XP. She presented acute paralysis of the third cranial nerve with cutaneous anesthesia. Nuclear magnetic resonance imaging revealed an intracranial tumor. She underwent surgery with incomplete tumor resection; anatomopathological study showed a schwannoma. Complementary radiosurgery was performed. The association between XP and neurological cancer is rare but not impossible. A priori, it would be assumed that the major medical outcome of hereditary deficiencies in DNA repair processes would be an increased risk of cancer. Indeed, there is an increased risk of cancer in several known DNA repair deficiencies including XP.

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