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Ocular Cicatricial Pemphigoid, Sjögren’s Syndrome, and Hashimoto’s Thyroiditis as a Multiple Autoimmune Syndrome: A case report
PURPOSE: To present a rare and novel association of Ocular Cicatricial Pemphigoid, Sjögren’s Syndrome, and Hashimoto’s Thyroiditis as a Multiple Autoimmune Syndrome. CASE REPORT: A 43-year-old Colombian female, presented with corneal ulcers, associated with trichiasis. At the ophthalmological examin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294440/ https://www.ncbi.nlm.nih.gov/pubmed/33601905 http://dx.doi.org/10.1177/1120672121996637 |
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author | Cifuentes-González, Carlos Amaris-Martínez, Stefania Reyes-Guanes, Juliana Uribe-Reina, Pilar de-la-Torre, Alejandra |
author_facet | Cifuentes-González, Carlos Amaris-Martínez, Stefania Reyes-Guanes, Juliana Uribe-Reina, Pilar de-la-Torre, Alejandra |
author_sort | Cifuentes-González, Carlos |
collection | PubMed |
description | PURPOSE: To present a rare and novel association of Ocular Cicatricial Pemphigoid, Sjögren’s Syndrome, and Hashimoto’s Thyroiditis as a Multiple Autoimmune Syndrome. CASE REPORT: A 43-year-old Colombian female, presented with corneal ulcers, associated with trichiasis. At the ophthalmological examination forniceal shortening OU and symblepharon OD was found. Conjunctival biopsy was performed, evidencing linear deposition of IgG and IgA antibodies along the basement membrane of the conjunctiva, confirming Ocular Cicatricial Pemphigoid diagnosis. After 12 years, the patient presented constitutional symptoms, xerostomia, and worsening of xerophthalmia. Laboratory tests showed positive Anti-TG, Anti-TPO, Anti-Ro, and Anti-La antibodies, and salivary gland biopsy was consistent with Sjögren’s Syndrome. Due to these findings, Hashimoto’s Thyroiditis and Sjögren’s Syndrome were diagnosed, defining a Multiple Autoimmune Syndrome. CONCLUSION: A novel association of Multiple Autoimmune Syndrome is presented in this case. Ophthalmologists and other specialists involved in the evaluation and treatment of patients with autoimmune diseases, should be aware of this clinical presentation. A multidisciplinary approach in this condition is important for optimum treatment instauration and follow-up, in order to prevent complications. |
format | Online Article Text |
id | pubmed-9294440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-92944402022-07-20 Ocular Cicatricial Pemphigoid, Sjögren’s Syndrome, and Hashimoto’s Thyroiditis as a Multiple Autoimmune Syndrome: A case report Cifuentes-González, Carlos Amaris-Martínez, Stefania Reyes-Guanes, Juliana Uribe-Reina, Pilar de-la-Torre, Alejandra Eur J Ophthalmol Case Reports PURPOSE: To present a rare and novel association of Ocular Cicatricial Pemphigoid, Sjögren’s Syndrome, and Hashimoto’s Thyroiditis as a Multiple Autoimmune Syndrome. CASE REPORT: A 43-year-old Colombian female, presented with corneal ulcers, associated with trichiasis. At the ophthalmological examination forniceal shortening OU and symblepharon OD was found. Conjunctival biopsy was performed, evidencing linear deposition of IgG and IgA antibodies along the basement membrane of the conjunctiva, confirming Ocular Cicatricial Pemphigoid diagnosis. After 12 years, the patient presented constitutional symptoms, xerostomia, and worsening of xerophthalmia. Laboratory tests showed positive Anti-TG, Anti-TPO, Anti-Ro, and Anti-La antibodies, and salivary gland biopsy was consistent with Sjögren’s Syndrome. Due to these findings, Hashimoto’s Thyroiditis and Sjögren’s Syndrome were diagnosed, defining a Multiple Autoimmune Syndrome. CONCLUSION: A novel association of Multiple Autoimmune Syndrome is presented in this case. Ophthalmologists and other specialists involved in the evaluation and treatment of patients with autoimmune diseases, should be aware of this clinical presentation. A multidisciplinary approach in this condition is important for optimum treatment instauration and follow-up, in order to prevent complications. SAGE Publications 2021-02-18 2022-07 /pmc/articles/PMC9294440/ /pubmed/33601905 http://dx.doi.org/10.1177/1120672121996637 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Reports Cifuentes-González, Carlos Amaris-Martínez, Stefania Reyes-Guanes, Juliana Uribe-Reina, Pilar de-la-Torre, Alejandra Ocular Cicatricial Pemphigoid, Sjögren’s Syndrome, and Hashimoto’s Thyroiditis as a Multiple Autoimmune Syndrome: A case report |
title | Ocular Cicatricial Pemphigoid, Sjögren’s Syndrome, and Hashimoto’s
Thyroiditis as a Multiple Autoimmune Syndrome: A case report |
title_full | Ocular Cicatricial Pemphigoid, Sjögren’s Syndrome, and Hashimoto’s
Thyroiditis as a Multiple Autoimmune Syndrome: A case report |
title_fullStr | Ocular Cicatricial Pemphigoid, Sjögren’s Syndrome, and Hashimoto’s
Thyroiditis as a Multiple Autoimmune Syndrome: A case report |
title_full_unstemmed | Ocular Cicatricial Pemphigoid, Sjögren’s Syndrome, and Hashimoto’s
Thyroiditis as a Multiple Autoimmune Syndrome: A case report |
title_short | Ocular Cicatricial Pemphigoid, Sjögren’s Syndrome, and Hashimoto’s
Thyroiditis as a Multiple Autoimmune Syndrome: A case report |
title_sort | ocular cicatricial pemphigoid, sjögren’s syndrome, and hashimoto’s
thyroiditis as a multiple autoimmune syndrome: a case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294440/ https://www.ncbi.nlm.nih.gov/pubmed/33601905 http://dx.doi.org/10.1177/1120672121996637 |
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