Ectopic Decidualization: A Forgotten Entity

Detalhes bibliográficos
Autor(a) principal: Mendes, Joana
Data de Publicação: 2016
Outros Autores: Costa, Antónia
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6466
Resumo: Introduction: Although ectopic decidualization is an entity often underdiagnosed, it may have adverse clinical impact on maternal-fetal morbimortality. The objective of this study was to review the scientific evidence regarding the etiology, clinical features, diagnosis and therapeutic approach on this issue.Material and Methods: The search for this literature review was conducted in PubMed, Web of Science and Scopus, through the query (‘deciduosis’ OR ‘ectopic decidualization’ OR ‘ectopic decidua’ OR ‘ectopic decidua reaction’), considering articles of all evidence levels published up to 31/06/2014.Results: Ectopic decidualization is, usually, a benign condition, asymptomatic and does not require therapeutic intervention. It occurs mostly during pregnancy, with complete regression in the postpartum period. The frequency of the diagnosis depends on the clinical suspicion and its location, being the omentum and the ovary the most common sites. When symptomatic, the main clinical manifestations are genital bleeding and hemoperitoneum. Differential diagnosis includes malignant disease and histopathological confirmation is essential in these situations. The low index of suspicion may lead to a biopsy, which can have serious adverse outcomes due to the high friability of these lesions.Discussion and Conclusion: The recognition of this entity and its clinical features are essential for the management of these patients. On one side this allows an early and proper medical approach in severe cases, on the other side (the majority of cases) maintaining an expectant attitude avoiding iatrogeny, does not compromise, in most cases, the favorable outcome of ectopic decidualization.
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spelling Ectopic Decidualization: A Forgotten EntityDecidualização Ectópica: Uma Entidade EsquecidaDeciduaPregnancyPregnancy Complications.Complicações na GravidezDecíduaGravidez.Introduction: Although ectopic decidualization is an entity often underdiagnosed, it may have adverse clinical impact on maternal-fetal morbimortality. The objective of this study was to review the scientific evidence regarding the etiology, clinical features, diagnosis and therapeutic approach on this issue.Material and Methods: The search for this literature review was conducted in PubMed, Web of Science and Scopus, through the query (‘deciduosis’ OR ‘ectopic decidualization’ OR ‘ectopic decidua’ OR ‘ectopic decidua reaction’), considering articles of all evidence levels published up to 31/06/2014.Results: Ectopic decidualization is, usually, a benign condition, asymptomatic and does not require therapeutic intervention. It occurs mostly during pregnancy, with complete regression in the postpartum period. The frequency of the diagnosis depends on the clinical suspicion and its location, being the omentum and the ovary the most common sites. When symptomatic, the main clinical manifestations are genital bleeding and hemoperitoneum. Differential diagnosis includes malignant disease and histopathological confirmation is essential in these situations. The low index of suspicion may lead to a biopsy, which can have serious adverse outcomes due to the high friability of these lesions.Discussion and Conclusion: The recognition of this entity and its clinical features are essential for the management of these patients. On one side this allows an early and proper medical approach in severe cases, on the other side (the majority of cases) maintaining an expectant attitude avoiding iatrogeny, does not compromise, in most cases, the favorable outcome of ectopic decidualization.Introdução: Apesar da decidualização ectópica ser uma entidade frequentemente subdiagnosticada, pode ter impacto clínico adverso na morbimortalidade materno-fetal. O objetivo deste trabalho foi rever a evidência científica relativa a etiopatogenia, clínica, abordagem diagnóstica e terapêutica sobre esta temática.Material e Métodos: A pesquisa bibliográfica foi realizada na PubMed, Web of Science e Scopus, através da query (‘deciduosis’ OR ‘ectopic decidualization’ OR ‘ectopic decidua’ OR ‘ectopic decidua reaction’), incluindo-se artigos publicados até 31/6/2014 e de todos os níveis de evidência.Resultados: A decidualização ectópica, geralmente, representa uma condição benigna, assintomática e sem necessidade de intervenção terapêutica. Encontra-se, maioritariamente, associada à gravidez, com regressão completa no período pós-parto. A frequência do seu diagnóstico depende da suspeição clínica, bem como do local onde surge, sendo o omento e o ovário os locais mais comuns. Quando sintomática, as principais manifestações clínicas são quadros hemorrágicos, nomeadamente hemorragia genital e hemoperitoneu. Os diagnósticos diferenciais incluem patologia maligna, sendo essencial, nestas situações, a confirmação histopatológica. O baixo índice de suspeição clínica pode levar à realização de biópsia, que pode acarretar impacto adverso grave devido à elevada friabilidade destas lesões.Discussão e Conclusão: O reconhecimento desta entidade e das suas características clínicas torna-se essencial na conduta destas doentes. Tal permite por um lado a abordagem médica precoce e adequada nos casos graves, e por outro lado (na maioria dos casos) manter a atitude expectante minimizando a iatrogenia, mantendo o desfecho favorável da decidualização ectópica.Ordem dos Médicos2016-01-29info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfapplication/mswordapplication/mswordapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6466oai:ojs.www.actamedicaportuguesa.com:article/6466Acta Médica Portuguesa; Vol. 29 No. 1 (2016): January; 63-72Acta Médica Portuguesa; Vol. 29 N.º 1 (2016): Janeiro; 63-721646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6466https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6466/4557https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6466/7798https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6466/7799https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/6466/7826Direitos de Autor (c) 2016 Copyright © Ordem dos Médicos 2016info:eu-repo/semantics/openAccessMendes, JoanaCosta, Antónia2022-12-20T11:04:52Zoai:ojs.www.actamedicaportuguesa.com:article/6466Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:19:18.916687Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Ectopic Decidualization: A Forgotten Entity
Decidualização Ectópica: Uma Entidade Esquecida
title Ectopic Decidualization: A Forgotten Entity
spellingShingle Ectopic Decidualization: A Forgotten Entity
Mendes, Joana
Decidua
Pregnancy
Pregnancy Complications.
Complicações na Gravidez
Decídua
Gravidez.
title_short Ectopic Decidualization: A Forgotten Entity
title_full Ectopic Decidualization: A Forgotten Entity
title_fullStr Ectopic Decidualization: A Forgotten Entity
title_full_unstemmed Ectopic Decidualization: A Forgotten Entity
title_sort Ectopic Decidualization: A Forgotten Entity
author Mendes, Joana
author_facet Mendes, Joana
Costa, Antónia
author_role author
author2 Costa, Antónia
author2_role author
dc.contributor.author.fl_str_mv Mendes, Joana
Costa, Antónia
dc.subject.por.fl_str_mv Decidua
Pregnancy
Pregnancy Complications.
Complicações na Gravidez
Decídua
Gravidez.
topic Decidua
Pregnancy
Pregnancy Complications.
Complicações na Gravidez
Decídua
Gravidez.
description Introduction: Although ectopic decidualization is an entity often underdiagnosed, it may have adverse clinical impact on maternal-fetal morbimortality. The objective of this study was to review the scientific evidence regarding the etiology, clinical features, diagnosis and therapeutic approach on this issue.Material and Methods: The search for this literature review was conducted in PubMed, Web of Science and Scopus, through the query (‘deciduosis’ OR ‘ectopic decidualization’ OR ‘ectopic decidua’ OR ‘ectopic decidua reaction’), considering articles of all evidence levels published up to 31/06/2014.Results: Ectopic decidualization is, usually, a benign condition, asymptomatic and does not require therapeutic intervention. It occurs mostly during pregnancy, with complete regression in the postpartum period. The frequency of the diagnosis depends on the clinical suspicion and its location, being the omentum and the ovary the most common sites. When symptomatic, the main clinical manifestations are genital bleeding and hemoperitoneum. Differential diagnosis includes malignant disease and histopathological confirmation is essential in these situations. The low index of suspicion may lead to a biopsy, which can have serious adverse outcomes due to the high friability of these lesions.Discussion and Conclusion: The recognition of this entity and its clinical features are essential for the management of these patients. On one side this allows an early and proper medical approach in severe cases, on the other side (the majority of cases) maintaining an expectant attitude avoiding iatrogeny, does not compromise, in most cases, the favorable outcome of ectopic decidualization.
publishDate 2016
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dc.rights.driver.fl_str_mv Direitos de Autor (c) 2016 Copyright © Ordem dos Médicos 2016
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dc.publisher.none.fl_str_mv Ordem dos Médicos
publisher.none.fl_str_mv Ordem dos Médicos
dc.source.none.fl_str_mv Acta Médica Portuguesa; Vol. 29 No. 1 (2016): January; 63-72
Acta Médica Portuguesa; Vol. 29 N.º 1 (2016): Janeiro; 63-72
1646-0758
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