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A case of pseudo-pseudo Meigs’ syndrome

Here we report a case of a patient with systemic lupus erythematosus presenting with pseudo-pseudo Meigs’ syndrome (PPMS): a triad of pleural effusion, ascites and raised CA-125. There have only been nine other cases reported in the literature. To our knowledge, this is the first to have an oesophag...

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Detalles Bibliográficos
Autores principales: Ahmed, Omnya, Malley, Tamir, Kitchen, Joanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355105/
https://www.ncbi.nlm.nih.gov/pubmed/30740231
http://dx.doi.org/10.1093/omcr/omy136
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author Ahmed, Omnya
Malley, Tamir
Kitchen, Joanne
author_facet Ahmed, Omnya
Malley, Tamir
Kitchen, Joanne
author_sort Ahmed, Omnya
collection PubMed
description Here we report a case of a patient with systemic lupus erythematosus presenting with pseudo-pseudo Meigs’ syndrome (PPMS): a triad of pleural effusion, ascites and raised CA-125. There have only been nine other cases reported in the literature. To our knowledge, this is the first to have an oesophago-gastro-duodenoscopy and liver biopsy as part of the diagnostic work up. Its mechanism of action is not yet fully understood but PPMS is a treatable condition that is responsive to immunosuppression. It is therefore important to consider it in patients presenting like this, where alternative diagnoses, including malignancy, have been ruled out.
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spelling pubmed-63551052019-02-08 A case of pseudo-pseudo Meigs’ syndrome Ahmed, Omnya Malley, Tamir Kitchen, Joanne Oxf Med Case Reports Case Report Here we report a case of a patient with systemic lupus erythematosus presenting with pseudo-pseudo Meigs’ syndrome (PPMS): a triad of pleural effusion, ascites and raised CA-125. There have only been nine other cases reported in the literature. To our knowledge, this is the first to have an oesophago-gastro-duodenoscopy and liver biopsy as part of the diagnostic work up. Its mechanism of action is not yet fully understood but PPMS is a treatable condition that is responsive to immunosuppression. It is therefore important to consider it in patients presenting like this, where alternative diagnoses, including malignancy, have been ruled out. Oxford University Press 2019-04-29 /pmc/articles/PMC6355105/ /pubmed/30740231 http://dx.doi.org/10.1093/omcr/omy136 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Ahmed, Omnya
Malley, Tamir
Kitchen, Joanne
A case of pseudo-pseudo Meigs’ syndrome
title A case of pseudo-pseudo Meigs’ syndrome
title_full A case of pseudo-pseudo Meigs’ syndrome
title_fullStr A case of pseudo-pseudo Meigs’ syndrome
title_full_unstemmed A case of pseudo-pseudo Meigs’ syndrome
title_short A case of pseudo-pseudo Meigs’ syndrome
title_sort case of pseudo-pseudo meigs’ syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6355105/
https://www.ncbi.nlm.nih.gov/pubmed/30740231
http://dx.doi.org/10.1093/omcr/omy136
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