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[Polymorphism and differential diagnosis of neonatal lupus erythematosus]. / Polymorphisme et diagnostics différentiels du lupus érythémateux néonatal.
Blanc, J; Bodak, N; Saada, V; Zavaro, A; Bagot, M; Petit, A; Bourrat, E.
Afiliação
  • Blanc J; Service de dermatologie, hôpital Robert-Debré, 75019 Paris, France. Electronic address: jlz.blanc@laposte.net.
  • Bodak N; Service de dermatologie, hôpital Trousseau, 75012 Paris, France.
  • Saada V; Service de dermatologie, hôpital St Louis, 75010 Paris, France.
  • Zavaro A; Cabinet médical, 94170 Le-Perreux-sur-Marne, France.
  • Bagot M; Service de dermatologie, hôpital St Louis, 75010 Paris, France.
  • Petit A; Service de dermatologie, hôpital St Louis, 75010 Paris, France.
  • Bourrat E; Service de dermatologie, hôpital Robert-Debré, 75019 Paris, France.
Ann Dermatol Venereol ; 147(4): 258-264, 2020 Apr.
Article em Fr | MEDLINE | ID: mdl-32171550
ABSTRACT

INTRODUCTION:

Neonatal lupus erythematosus (NEL) is a rare condition secondary to transplacental transfer of maternal anti-nuclear antibodies, generally anti-Ro/SSA. The most common signs are dermatological and cardiac. The most frequently reported clinical association is periorbital erythema, known as "owl eye", and bipolar erythematous maculopapular plaques with fine scales. However, many semiological variants can result in diagnostic errors or delays. PATIENTS AND

METHODS:

This was a single-centre retrospective observational study collating all cases of NEL seen at paediatric dermatology consultations between 2010 and 2018. The diagnosis of NEL was confirmed by the presence of specific antinuclear antibodies (ANA) in the mother. The aim was to describe the different clinical forms of NEL and to discuss differential diagnosis. RESULTS AND

DISCUSSION:

We identified ten cases of NEL, all addressed without diagnosis or with misdiagnosis. They were divided into 3 groups based on the semiology of skin lesions 5 presented inflammatory macular papules on the cephalic extremity and head; 3 presented acquired periorbital depigmentation; 2 presented atrophic and diffuse livedoid lesions. None had heart disease and associated haematological and hepatic damage was mild. Spontaneous remission was seen in all cases before the age of 6 months. The mothers, who were generally symptom-free or paucisymptomatic, presented anti-Ro/SSA NAAs.

CONCLUSION:

Recognition of the different clinical forms of NEL enables early institution of suitable therapy and monitoring of subsequent pregnancies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lúpus Eritematoso Sistêmico Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Newborn / Pregnancy Idioma: Fr Revista: Ann Dermatol Venereol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lúpus Eritematoso Sistêmico Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Newborn / Pregnancy Idioma: Fr Revista: Ann Dermatol Venereol Ano de publicação: 2020 Tipo de documento: Article