Dyskeratosis Congenita / 대한피부과학회지
Korean Journal of Dermatology
;
: 377-380, 2003.
Article
Dans Coréen
| WPRIM
| ID: wpr-110714
ABSTRACT
Dyskeratosis congenita is a rare multisystemic genodermatosis of ectodermal dysplasia, and is characterized by the diagnostic triad consisting of reticulated hyperpigmentation, dystrophic nails, and leukoplakia. Complications such a malignancy and bone marrow involvement will be predisposition. A 44-year-old male was presented with reticulated hyperpigmentation, nail dystrophy, oral leukoplakia, mild hyperkeratosis of the palms and soles, and short stature. His brothers were presented with reticulated hyperpigmentation and nail dystrophy, and underwent a surgical operation due to oral cavity cancer. The histopathological findings taken from the reticulated lesion showed epidermal thinning and a mild inflammatory cell infiltration with melanophages in the dermis. We report a typical case of dyskeratosis congenita in a male with family history.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Moelle osseuse
/
Dysplasie ectodermique
/
Leucoplasie buccale
/
Hyperpigmentation
/
Dyskératose congénitale
/
Derme
/
Fratrie
/
Leucoplasie
/
Bouche
Limites du sujet:
Adulte
/
Humains
/
Mâle
langue:
Coréen
Texte intégral:
Korean Journal of Dermatology
Année:
2003
Type:
Article
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