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Fulminant Neurologic Manifestation of Sjogren’s Syndrome: A Case Report

Sjogren's syndrome (SS) is an autoimmune disorder characterized by the destruction of exocrine glands by lymphocytic infiltration. Children and teenagers are less commonly affected. The initial symptoms of SS in teenagers might vary, depending on whether parotitis or other systemic organ involv...

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Autores principales: Laxmidhar, Rosy M, Laxmidhar, Fehmida, Shastri, Kavit, Patel, Sahil, Patel, Shivani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460263/
https://www.ncbi.nlm.nih.gov/pubmed/37637659
http://dx.doi.org/10.7759/cureus.42604
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author Laxmidhar, Rosy M
Laxmidhar, Fehmida
Shastri, Kavit
Patel, Sahil
Patel, Shivani
author_facet Laxmidhar, Rosy M
Laxmidhar, Fehmida
Shastri, Kavit
Patel, Sahil
Patel, Shivani
author_sort Laxmidhar, Rosy M
collection PubMed
description Sjogren's syndrome (SS) is an autoimmune disorder characterized by the destruction of exocrine glands by lymphocytic infiltration. Children and teenagers are less commonly affected. The initial symptoms of SS in teenagers might vary, depending on whether parotitis or other systemic organ involvement is present. Glandular involvement with the clinical hallmarks of dry eyes and dry mouth is common. Our case report is about a young woman who was admitted with acute flaccid paralysis and severe respiratory distress with extremely low serum potassium; further investigation revealed distal renal tubular acidosis. The patient was ultimately diagnosed with primary SS with high levels of SS-a/SS-b antibodies and a positive Schirmer's test. Our case demonstrates that hypokalemic paralysis can be a manifestation of SS, even though it is a rare cause.
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spelling pubmed-104602632023-08-27 Fulminant Neurologic Manifestation of Sjogren’s Syndrome: A Case Report Laxmidhar, Rosy M Laxmidhar, Fehmida Shastri, Kavit Patel, Sahil Patel, Shivani Cureus Internal Medicine Sjogren's syndrome (SS) is an autoimmune disorder characterized by the destruction of exocrine glands by lymphocytic infiltration. Children and teenagers are less commonly affected. The initial symptoms of SS in teenagers might vary, depending on whether parotitis or other systemic organ involvement is present. Glandular involvement with the clinical hallmarks of dry eyes and dry mouth is common. Our case report is about a young woman who was admitted with acute flaccid paralysis and severe respiratory distress with extremely low serum potassium; further investigation revealed distal renal tubular acidosis. The patient was ultimately diagnosed with primary SS with high levels of SS-a/SS-b antibodies and a positive Schirmer's test. Our case demonstrates that hypokalemic paralysis can be a manifestation of SS, even though it is a rare cause. Cureus 2023-07-28 /pmc/articles/PMC10460263/ /pubmed/37637659 http://dx.doi.org/10.7759/cureus.42604 Text en Copyright © 2023, Laxmidhar et al. https://creativecommons.org/licenses/by/3.0/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 author and source are credited.
spellingShingle Internal Medicine
Laxmidhar, Rosy M
Laxmidhar, Fehmida
Shastri, Kavit
Patel, Sahil
Patel, Shivani
Fulminant Neurologic Manifestation of Sjogren’s Syndrome: A Case Report
title Fulminant Neurologic Manifestation of Sjogren’s Syndrome: A Case Report
title_full Fulminant Neurologic Manifestation of Sjogren’s Syndrome: A Case Report
title_fullStr Fulminant Neurologic Manifestation of Sjogren’s Syndrome: A Case Report
title_full_unstemmed Fulminant Neurologic Manifestation of Sjogren’s Syndrome: A Case Report
title_short Fulminant Neurologic Manifestation of Sjogren’s Syndrome: A Case Report
title_sort fulminant neurologic manifestation of sjogren’s syndrome: a case report
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460263/
https://www.ncbi.nlm.nih.gov/pubmed/37637659
http://dx.doi.org/10.7759/cureus.42604
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