A Case of Type 1 Pachyonychia Congenita (Jadassohn-Lewandowsky Syndrome) / 대한피부과학회지
Korean Journal of Dermatology
; : 265-268, 2011.
Article
em Ko
| WPRIM
| ID: wpr-177816
Biblioteca responsável:
WPRO
ABSTRACT
Pachyonychia congenita (PC) is characterized by hypertrophic nail dystrophy, focal palmoplantar keratoderma and blistering, oral leukokeratosis, cyst formation, palmoplantar hyperhydrosis, and follicular keratoses on the trunk and extremities. PC is diagnosed by clinical findings and molecular genetic studies. A 26-year-old man presented with hypertrophic nail dystrophy and subungual debris of all 20 nails, hyperkeratotic plaques on the heels of both soles, and oral leukokeratosis. He had no family history of similar clinical findings. The patient's clinical presentation and history were consistent with PC. Herein we report on a rare case of pachyonychia congenita with a review of literature.
Palavras-chave
Texto completo:
1
Índice:
WPRIM
Assunto principal:
Leucoplasia Oral
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Calcanhar
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Vesícula
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Ceratodermia Palmar e Plantar
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Paquioníquia Congênita
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Extremidades
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Ceratose
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Biologia Molecular
/
Unhas
Limite:
Adult
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Humans
Idioma:
Ko
Revista:
Korean Journal of Dermatology
Ano de publicação:
2011
Tipo de documento:
Article