Oral Oncology Reports (Jun 2023)

Oral leukoplakia in adolescents: Attention to differential diagnosis of inherited genetic syndromes with emphasis on dyskeratosis congenita and Fanconi anemia

  • Shiyi Chen,
  • Chenbin Xu,
  • Yizhen Wu,
  • Wei Liu,
  • Xi Yang

Journal volume & issue
Vol. 6
p. 100043

Abstract

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Among inherited cancer syndromes, dyskeratosis congenita (DKC) and Fanconi anemia (FA) are most closely associated with the onset and progression of oral potentially malignant disorders (OPMD) with emphasis on oral leukoplakia (OLK) in adolescents. DKC often arises early and should always be considered and excluded in a child presenting with OLK. A total of 30 (41.1%) of 73 FA patients compatible with OPMD further developed into oral cancer at the young age (10–30 years old) are identified in literature. Individuals with inherited genetic syndromes, especially DKC and FA, should be a target young population with increased risk of OPMD onset and further progression to oral cancer. Hence, it is suggested that OLK in adolescents should pay attention to differential diagnosis of inherited genetic syndromes, mainly DKC and FA.

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