Literature DB >> 10209473

Squamous cell carcinoma of the tongue in a patient with Rothmund-Thomson syndrome.

S Marín-Bertolín1, J Amorrortu-Velayos, A Aliaga Boniche.   

Abstract

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.

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Year:  1998        PMID: 10209473     DOI: 10.1054/bjps.1998.0050

Source DB:  PubMed          Journal:  Br J Plast Surg        ISSN: 0007-1226


  4 in total

1.  Therapy-resistant leg ulcer in a patient with Rothmund-Thomson syndrome.

Authors:  Ilknur Altunay; Neslihan Fisek; Gonca Gokdemir; Damlanur Sakız; Umran Cetincelik
Journal:  Int Wound J       Date:  2010-09-21       Impact factor: 3.315

2.  Schimke Immunoosseous Dysplasia associated with undifferentiated carcinoma and a novel SMARCAL1 mutation in a child.

Authors:  Clinton Carroll; Akosua Badu-Nkansah; Tracy Hunley; Alireza Baradaran-Heravi; David Cortez; Haydar Frangoul
Journal:  Pediatr Blood Cancer       Date:  2013-04-29       Impact factor: 3.167

Review 3.  Non-Melanoma Skin Cancers and Other Cutaneous Manifestations in Bone Marrow Failure Syndromes and Rare DNA Repair Disorders.

Authors:  Jennie Vagher; Amanda Gammon; Wendy Kohlmann; Joanne Jeter
Journal:  Front Oncol       Date:  2022-03-10       Impact factor: 6.244

4.  Oral findings of rothmund-thomson syndrome.

Authors:  Emin Murat Canger; Peruze Celenk; Inci Devrim; Aysun Avşar
Journal:  Case Rep Dent       Date:  2013-11-30
  4 in total

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