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Autoimmune hypophysitis and viral infection in a pregnant woman: a challengeable case

The aim of this study is to report a challengeable and rare case of autoimmune hypophysitis possibly induced by viral infections. A young pregnant female developed optic neuropathy due to enlarged sellar mass responsible for hypopituitarism. Investigations exclude neoplasia and systemic diseases. Hi...

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Detalles Bibliográficos
Autor principal: Benabderrahim, Kais
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388598/
https://www.ncbi.nlm.nih.gov/pubmed/32774605
http://dx.doi.org/10.11604/pamj.2020.36.28.22454
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author Benabderrahim, Kais
author_facet Benabderrahim, Kais
author_sort Benabderrahim, Kais
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description The aim of this study is to report a challengeable and rare case of autoimmune hypophysitis possibly induced by viral infections. A young pregnant female developed optic neuropathy due to enlarged sellar mass responsible for hypopituitarism. Investigations exclude neoplasia and systemic diseases. High level of sedimentation rate and magnetic resonance imaging (MRI) findings supported the diagnosis of autoimmune hypophysitis. The patient reported a history of bronchitis treated with antibiotics and corticosteroids and positive serologies for hepatitis B antigen (Hbs antigen), herpes simplex 1 and rubella. Final examination showed complete recovery of visual function and sellar archnoidocele after antiviral treatment and mild dose of corticosteroids.
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spelling pubmed-73885982020-08-07 Autoimmune hypophysitis and viral infection in a pregnant woman: a challengeable case Benabderrahim, Kais Pan Afr Med J Case Report The aim of this study is to report a challengeable and rare case of autoimmune hypophysitis possibly induced by viral infections. A young pregnant female developed optic neuropathy due to enlarged sellar mass responsible for hypopituitarism. Investigations exclude neoplasia and systemic diseases. High level of sedimentation rate and magnetic resonance imaging (MRI) findings supported the diagnosis of autoimmune hypophysitis. The patient reported a history of bronchitis treated with antibiotics and corticosteroids and positive serologies for hepatitis B antigen (Hbs antigen), herpes simplex 1 and rubella. Final examination showed complete recovery of visual function and sellar archnoidocele after antiviral treatment and mild dose of corticosteroids. The African Field Epidemiology Network 2020-05-21 /pmc/articles/PMC7388598/ /pubmed/32774605 http://dx.doi.org/10.11604/pamj.2020.36.28.22454 Text en © Kais Benabderrahim et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Benabderrahim, Kais
Autoimmune hypophysitis and viral infection in a pregnant woman: a challengeable case
title Autoimmune hypophysitis and viral infection in a pregnant woman: a challengeable case
title_full Autoimmune hypophysitis and viral infection in a pregnant woman: a challengeable case
title_fullStr Autoimmune hypophysitis and viral infection in a pregnant woman: a challengeable case
title_full_unstemmed Autoimmune hypophysitis and viral infection in a pregnant woman: a challengeable case
title_short Autoimmune hypophysitis and viral infection in a pregnant woman: a challengeable case
title_sort autoimmune hypophysitis and viral infection in a pregnant woman: a challengeable case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388598/
https://www.ncbi.nlm.nih.gov/pubmed/32774605
http://dx.doi.org/10.11604/pamj.2020.36.28.22454
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