Rothmund-Thomson syndrome is a rare autosomal recessive genodermatosis characterised by poikilodermatous skin changes that appear in childhood. Patients exhibit variable additional features including juvenile cataracts, skeletal abnormalities and a higher than expected incidence of malignancies. We report a case of squamous cell carcinoma of the tongue in a 37-year-old Rothmund-Thomson syndrome patient and review the natural history of this rare disease, given that the patient was diagnosed with Rothmund-Thomson syndrome at the age of 8 years and was first reported in 1975.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1054/bjps.1998.0050 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!