Dyskeratosis congenita. Report of a case with literature review

Ajit Auluck

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

Leukoplakic lesion is not uncommon in clinical practice but its occurrence as a component of a syndrome is rare. Dyskeratosis congenita is a rare genodermatosis, which is characterized by triad of skin pigmentation, nail dystrophy and leukoplakic lesion in the oral cavity. It is important for dentists to now about Dyskeratosis Congenita because these leukoplakic lesions can spontaneously undergo malignant transformation. Majority of cases have been reported in dermatology or pediatrics literature whereas only few reports have appeared in dental literature. The purpose of reporting this case with review of recent literature is to create better awareness among dentists about the multisystem manifestations and oro-dental abnormalities of this fatal condition that can aid clinicians in early diagnosis. A case of 26 year old male is reported with details of differential diagnosis, importance of hematological investigations, periodic biopsies and current concepts in management of such patients are briefly reviewed.

Original languageEnglish
JournalMedicina Oral, Patologia Oral y Cirugia Bucal
Volume12
Issue number5
Publication statusPublished - 01-09-2007
Externally publishedYes

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Dyskeratosis Congenita
Leukoplakia
Dentists
Tooth Abnormalities
Skin Pigmentation
Nails
Dermatology
Mouth
Early Diagnosis
Tooth
Differential Diagnosis
Pediatrics
Biopsy

All Science Journal Classification (ASJC) codes

  • Surgery
  • Otorhinolaryngology
  • Dentistry(all)

Cite this

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Dyskeratosis congenita. Report of a case with literature review. / Auluck, Ajit.

In: Medicina Oral, Patologia Oral y Cirugia Bucal, Vol. 12, No. 5, 01.09.2007.

Research output: Contribution to journalArticle

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