Dyskeratosis congenita: a case report and review of literature
Dyskeratosis congenita (DC) is classically characterised by a mucocutaneous triad of reticulated poikiloderma, nail dystrophy and mucosal leukoplakia together with bone marrow failure and increased risk of malignancy1- 4. Due to its rarity and clinical heterogeneity it is not easily recognised and p...
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| Main Authors: | , |
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| Format: | Article |
| Language: | en |
| Published: |
Persatuan Dermatologi Malaysia
2014
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| Online Access: | http://psasir.upm.edu.my/id/eprint/37178/1/Dyskeratosis%20congenita.pdf http://psasir.upm.edu.my/id/eprint/37178/ http://www.dermatology.org.my/journal.htm |
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| Summary: | Dyskeratosis congenita (DC) is classically characterised by a mucocutaneous triad of reticulated poikiloderma, nail dystrophy and mucosal leukoplakia together with bone marrow failure and increased risk of malignancy1- 4. Due to its rarity and clinical heterogeneity it is not easily recognised and patients are often treated for other entities. We report a case of dyskeratosis congenita who presented to us with the classical triad in his late twenties after years of being treated as lichen planus. |
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