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Telangiectasia Occurred after Neonatal Lupus Erythematosus / 대한피부과학회지
Korean Journal of Dermatology ; : 297-300, 2017.
Article Dans Coréen | WPRIM | ID: wpr-165086
ABSTRACT
Neonatal lupus erythematosus (NLE) is an uncommon autoimmune disease that is associated with transplacental passage of maternal autoantibodies into the fetal circulation. It is commonly presented as multiple round, pink to red macules involving scalp, face and extremities. The characteristic skin lesions of NLE generally resolve without scarring within 6 months, but transient hyperpigmentation or hypopigmentation has been reported in some dark-skinned infants. We report a rare case of 3 year-old girl showing telangiectasia at the site of previous NLE lesions. In past history, at 2 days after birth, erythematous macules and patches on face and extremities had been presented and she was diagnosed as NLE in pediatrics. To our knowledge, it is the first report of residual telangiectasia after NLE in Korean dermatologic literature. Furthermore, we propose that dermatologists should consider the possibility of the cutaneous sequelae associated with NLE when encountering a child showing multiple telangiectasia.
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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Pédiatrie / Cuir chevelu / Peau / Autoanticorps / Maladies auto-immunes / Télangiectasie / Cicatrice / Hypopigmentation / Hyperpigmentation / Parturition Limites du sujet: Enfant / Femelle / Humains / Bébé langue: Coréen Texte intégral: Korean Journal of Dermatology Année: 2017 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Pédiatrie / Cuir chevelu / Peau / Autoanticorps / Maladies auto-immunes / Télangiectasie / Cicatrice / Hypopigmentation / Hyperpigmentation / Parturition Limites du sujet: Enfant / Femelle / Humains / Bébé langue: Coréen Texte intégral: Korean Journal of Dermatology Année: 2017 Type: Article