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Tolosa-Hunt Syndrome: A Case Report

Tolosa-Hunt Syndrome is a rare disease characterized by painful ophthalmoplegia affecting third, fourth, and/or sixth cranial nerve caused by non-specific inflammation in the cavernous sinus or superior orbital fissure of unknown etiology. We presented a 67-year-old female with Tolosa-Hunt Syndrome....

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Autores principales: Siddhanta, K.C., Shreeyanta, K.C., Kunwar, Prajjwal, Dhungana, Krishna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Journal of the Nepal Medical Association 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369562/
https://www.ncbi.nlm.nih.gov/pubmed/34508416
http://dx.doi.org/10.31729/jnma.5700
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author Siddhanta, K.C.
Shreeyanta, K.C.
Kunwar, Prajjwal
Dhungana, Krishna
author_facet Siddhanta, K.C.
Shreeyanta, K.C.
Kunwar, Prajjwal
Dhungana, Krishna
author_sort Siddhanta, K.C.
collection PubMed
description Tolosa-Hunt Syndrome is a rare disease characterized by painful ophthalmoplegia affecting third, fourth, and/or sixth cranial nerve caused by non-specific inflammation in the cavernous sinus or superior orbital fissure of unknown etiology. We presented a 67-year-old female with Tolosa-Hunt Syndrome. She had a right-sided headache and periorbital pain with double vision. Examination showed right-sided ptosis, right-sided trochlear and abducens nerve palsy, and partial right-sided oculomotor nerve palsy with hypoesthesia in the area of the ophthalmic division of the trigeminal nerve. Magnetic resonance imaging of head and orbit showed altered signal intensity changes in the optic nerve and lateral rectus muscle. After steroid therapy, pain and ptosis were significantly improved in 72 hours. Tolosa-Hunt Syndrome is a diagnosis of exclusion, with clinical presentation, normal investigations, magnetic resonance imaging findings, and response to steroid therapy crucial in making the diagnosis.
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spelling pubmed-83695622021-08-30 Tolosa-Hunt Syndrome: A Case Report Siddhanta, K.C. Shreeyanta, K.C. Kunwar, Prajjwal Dhungana, Krishna JNMA J Nepal Med Assoc Case Report Tolosa-Hunt Syndrome is a rare disease characterized by painful ophthalmoplegia affecting third, fourth, and/or sixth cranial nerve caused by non-specific inflammation in the cavernous sinus or superior orbital fissure of unknown etiology. We presented a 67-year-old female with Tolosa-Hunt Syndrome. She had a right-sided headache and periorbital pain with double vision. Examination showed right-sided ptosis, right-sided trochlear and abducens nerve palsy, and partial right-sided oculomotor nerve palsy with hypoesthesia in the area of the ophthalmic division of the trigeminal nerve. Magnetic resonance imaging of head and orbit showed altered signal intensity changes in the optic nerve and lateral rectus muscle. After steroid therapy, pain and ptosis were significantly improved in 72 hours. Tolosa-Hunt Syndrome is a diagnosis of exclusion, with clinical presentation, normal investigations, magnetic resonance imaging findings, and response to steroid therapy crucial in making the diagnosis. Journal of the Nepal Medical Association 2021-06 2021-06-30 /pmc/articles/PMC8369562/ /pubmed/34508416 http://dx.doi.org/10.31729/jnma.5700 Text en © The Author(s) 2018. https://creativecommons.org/licenses/by/4.0/This is an Open-Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Siddhanta, K.C.
Shreeyanta, K.C.
Kunwar, Prajjwal
Dhungana, Krishna
Tolosa-Hunt Syndrome: A Case Report
title Tolosa-Hunt Syndrome: A Case Report
title_full Tolosa-Hunt Syndrome: A Case Report
title_fullStr Tolosa-Hunt Syndrome: A Case Report
title_full_unstemmed Tolosa-Hunt Syndrome: A Case Report
title_short Tolosa-Hunt Syndrome: A Case Report
title_sort tolosa-hunt syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369562/
https://www.ncbi.nlm.nih.gov/pubmed/34508416
http://dx.doi.org/10.31729/jnma.5700
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