Neonatal lupus erythematosus: A narrative review

Bibliographic Details
Main Author: Marques, Ana Raquel
Publication Date: 2022
Other Authors: Rocha, Gustavo, Soares, Paulo, Rodrigues, Mariana, Pimenta, Joana
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://doi.org/10.25753/BirthGrowthMJ.v31.i4.27109
Summary: Introduction: Neonatal lupus erythematosus (NLE) is characterized by the transplacental passage of maternal antibodies, mainly anti-Sjogren’s syndrome A/Ro (anti-SSA/Ro) and anti-Sjogren’s syndrome B/La (anti-SSB/La), which bind to the developing fetal tissues. Seropositive mothers may have a diagnosed disease, such as Sjögren’s syndrome, systemic lupus erythematosus, or undifferentiated connective tissue disease, but in 25─60% of cases, they are asymptomatic at the time of childbirth. Objectives: This article aimed to provide a narrative review of the current state of knowledge on NLE. Development: The clinical spectrum of NLE includes both reversible and irreversible features. Reversible clinical features, like cutaneous lesions, hematological and pulmonary abnormalities, and hepatobiliary dysfunction, disappear spontaneously as autoantibody levels decrease in the bloodstream. The most commonly reported NLE manifestation is cardiac disease. Injury to the cardiac conduction tissue may lead to defects, such as congenital atrioventricular (AV) block, which is the most severe and, in some cases, lethal NLE manifestation. NLE may also have an impact on the myocardium and endocardium, with maternal antibodies being responsible for endocardial fibroelastosis. Immune-mediated AV block may benefit from in-utero treatment with steroids. Hydroxychloroquine may also be prescribed to women with immune-mediated disorders in the preconception period. Conclusions: The management of infants affected with NLE should be performed in a tertiary care center. Postnatal pacemaker insertion may be indicated in the presence of irreversible AV block or heart failure. Erythrocyte or platelet transfusions, corticosteroids, or intravenous immunoglobulin may be indicated to treat severe disease manifestations.
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spelling Neonatal lupus erythematosus: A narrative reviewLupus eritematoso neonatal: Uma revisão narrativaReview ArticlesIntroduction: Neonatal lupus erythematosus (NLE) is characterized by the transplacental passage of maternal antibodies, mainly anti-Sjogren’s syndrome A/Ro (anti-SSA/Ro) and anti-Sjogren’s syndrome B/La (anti-SSB/La), which bind to the developing fetal tissues. Seropositive mothers may have a diagnosed disease, such as Sjögren’s syndrome, systemic lupus erythematosus, or undifferentiated connective tissue disease, but in 25─60% of cases, they are asymptomatic at the time of childbirth. Objectives: This article aimed to provide a narrative review of the current state of knowledge on NLE. Development: The clinical spectrum of NLE includes both reversible and irreversible features. Reversible clinical features, like cutaneous lesions, hematological and pulmonary abnormalities, and hepatobiliary dysfunction, disappear spontaneously as autoantibody levels decrease in the bloodstream. The most commonly reported NLE manifestation is cardiac disease. Injury to the cardiac conduction tissue may lead to defects, such as congenital atrioventricular (AV) block, which is the most severe and, in some cases, lethal NLE manifestation. NLE may also have an impact on the myocardium and endocardium, with maternal antibodies being responsible for endocardial fibroelastosis. Immune-mediated AV block may benefit from in-utero treatment with steroids. Hydroxychloroquine may also be prescribed to women with immune-mediated disorders in the preconception period. Conclusions: The management of infants affected with NLE should be performed in a tertiary care center. Postnatal pacemaker insertion may be indicated in the presence of irreversible AV block or heart failure. Erythrocyte or platelet transfusions, corticosteroids, or intravenous immunoglobulin may be indicated to treat severe disease manifestations.Introdução: O lúpus eritematoso neonatal caracteriza-se pela passagem transplacentária de anticorpos maternos, maioritariamente anti-síndrome de Sjögren A/Ro (anti-SSA/Ro) e anti-síndrome de Sjögren B/La (anti-SSB/La), que se ligam aos tecidos fetais em desenvolvimento. Mães seropositivas podem ter doença diagnosticada, nomeadamente síndrome de Sjögren, lúpus eritematoso sistémico, ou doença indiferenciada do tecido conjuntivo, mas em 25─60% dos casos são assintomáticas à data do parto. Objetivos: O objetivo deste estudo foi fazer uma revisão narrativa sobre o estado da arte do lúpus eritematoso neonatal. Desenvolvimento: As características clínicas do lúpus neonatal podem ser reversíveis ou irreversíveis. As características reversíveis, como lesões cutâneas, alterações hematológicas ou pulmonares e disfunção hepatobiliar, desaparecem espontaneamente à medida que os níveis de anticorpos circulantes diminuem, geralmente nos primeiros 6 a 8 meses de vida. A manifestação mais frequente de lúpus neonatal é doença cardíaca. A lesão do tecido de condução cardíaco pode resultar em bloqueio atrioventricular (AV) congénito, que constitui a manifestação mais grave e em alguns casos fatal de lúpus neonatal. A doença pode também ter impacto no miocárdio e endocárdio, dado que os anticorpos maternos podem causar fibroelastose endocárdica. O bloqueio AV imunomediado pode beneficiar do tratamento in utero com corticoides. Mulheres com patologia imunomediada podem também receber hidroxicloroquina no período pré-concecional. Conclusões: A abordagem de recém-nascidos com lúpus neonatal deve ser feita num centro terciário. Em presença de bloqueio AV irreversível ou sinais de insuficiência cardíaca, pode ser necessária a colocação de pacemaker após o nascimento. As manifestações graves da doença podem necessitar de transfusões de eritrócitos ou plaquetas, corticosteroides ou imunoglobulina endovenosa.Unidade Local de Saúde de Santo António2022-12-27info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.25753/BirthGrowthMJ.v31.i4.27109eng2183-9417Marques, Ana RaquelRocha, GustavoSoares, PauloRodrigues, MarianaPimenta, Joanainfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-07T09:47:10Zoai:ojs.revistas.rcaap.pt:article/27109Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T14:39:48.302909Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Neonatal lupus erythematosus: A narrative review
Lupus eritematoso neonatal: Uma revisão narrativa
title Neonatal lupus erythematosus: A narrative review
spellingShingle Neonatal lupus erythematosus: A narrative review
Marques, Ana Raquel
Review Articles
title_short Neonatal lupus erythematosus: A narrative review
title_full Neonatal lupus erythematosus: A narrative review
title_fullStr Neonatal lupus erythematosus: A narrative review
title_full_unstemmed Neonatal lupus erythematosus: A narrative review
title_sort Neonatal lupus erythematosus: A narrative review
author Marques, Ana Raquel
author_facet Marques, Ana Raquel
Rocha, Gustavo
Soares, Paulo
Rodrigues, Mariana
Pimenta, Joana
author_role author
author2 Rocha, Gustavo
Soares, Paulo
Rodrigues, Mariana
Pimenta, Joana
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Marques, Ana Raquel
Rocha, Gustavo
Soares, Paulo
Rodrigues, Mariana
Pimenta, Joana
dc.subject.por.fl_str_mv Review Articles
topic Review Articles
description Introduction: Neonatal lupus erythematosus (NLE) is characterized by the transplacental passage of maternal antibodies, mainly anti-Sjogren’s syndrome A/Ro (anti-SSA/Ro) and anti-Sjogren’s syndrome B/La (anti-SSB/La), which bind to the developing fetal tissues. Seropositive mothers may have a diagnosed disease, such as Sjögren’s syndrome, systemic lupus erythematosus, or undifferentiated connective tissue disease, but in 25─60% of cases, they are asymptomatic at the time of childbirth. Objectives: This article aimed to provide a narrative review of the current state of knowledge on NLE. Development: The clinical spectrum of NLE includes both reversible and irreversible features. Reversible clinical features, like cutaneous lesions, hematological and pulmonary abnormalities, and hepatobiliary dysfunction, disappear spontaneously as autoantibody levels decrease in the bloodstream. The most commonly reported NLE manifestation is cardiac disease. Injury to the cardiac conduction tissue may lead to defects, such as congenital atrioventricular (AV) block, which is the most severe and, in some cases, lethal NLE manifestation. NLE may also have an impact on the myocardium and endocardium, with maternal antibodies being responsible for endocardial fibroelastosis. Immune-mediated AV block may benefit from in-utero treatment with steroids. Hydroxychloroquine may also be prescribed to women with immune-mediated disorders in the preconception period. Conclusions: The management of infants affected with NLE should be performed in a tertiary care center. Postnatal pacemaker insertion may be indicated in the presence of irreversible AV block or heart failure. Erythrocyte or platelet transfusions, corticosteroids, or intravenous immunoglobulin may be indicated to treat severe disease manifestations.
publishDate 2022
dc.date.none.fl_str_mv 2022-12-27
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dc.identifier.uri.fl_str_mv https://doi.org/10.25753/BirthGrowthMJ.v31.i4.27109
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dc.relation.none.fl_str_mv 2183-9417
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dc.publisher.none.fl_str_mv Unidade Local de Saúde de Santo António
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