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Extrapulmonary tuberculosis presenting as a cavernous sinus syndrome: Case report with review of existing literature

Tuberculoma involving the cavernous sinus is a rare presentation of CNS disease, with only twelve cases reported in previous literature. We report a case of a 48 year old woman who presented with a right cavernous sinus syndrome of 2 months duration. MRI showed a mass in the right cavernous sinus, a...

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Autores principales: Kapadia, Shashi, Patrawalla, Amee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735080/
https://www.ncbi.nlm.nih.gov/pubmed/26839786
http://dx.doi.org/10.1016/j.idcr.2014.10.010
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author Kapadia, Shashi
Patrawalla, Amee
author_facet Kapadia, Shashi
Patrawalla, Amee
author_sort Kapadia, Shashi
collection PubMed
description Tuberculoma involving the cavernous sinus is a rare presentation of CNS disease, with only twelve cases reported in previous literature. We report a case of a 48 year old woman who presented with a right cavernous sinus syndrome of 2 months duration. MRI showed a mass in the right cavernous sinus, and serologic workup revealed an elevated sedimentation rate and positive Quantiferon(®)-GOLD testing. 18-FDG PET-CT demonstrated a hypermetabolic 3 cm subcarinal lymph node, and lymph node biopsy showed caseating granuloma. Culture of lymphatic tissue grew drug-sensitive M. tuberculosis. The patient was treated with a non-standard 4-drug regimen and prednisone, with rapid improvement of symptoms and radiologic abnormalities. Total length of treatment was 12 months. In addition, we review the 12 cases found in literature, and discuss clinical features, diagnostic dilemmas, and approaches to treatment.
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spelling pubmed-47350802016-02-02 Extrapulmonary tuberculosis presenting as a cavernous sinus syndrome: Case report with review of existing literature Kapadia, Shashi Patrawalla, Amee IDCases Case Report Tuberculoma involving the cavernous sinus is a rare presentation of CNS disease, with only twelve cases reported in previous literature. We report a case of a 48 year old woman who presented with a right cavernous sinus syndrome of 2 months duration. MRI showed a mass in the right cavernous sinus, and serologic workup revealed an elevated sedimentation rate and positive Quantiferon(®)-GOLD testing. 18-FDG PET-CT demonstrated a hypermetabolic 3 cm subcarinal lymph node, and lymph node biopsy showed caseating granuloma. Culture of lymphatic tissue grew drug-sensitive M. tuberculosis. The patient was treated with a non-standard 4-drug regimen and prednisone, with rapid improvement of symptoms and radiologic abnormalities. Total length of treatment was 12 months. In addition, we review the 12 cases found in literature, and discuss clinical features, diagnostic dilemmas, and approaches to treatment. Elsevier 2014-11-04 /pmc/articles/PMC4735080/ /pubmed/26839786 http://dx.doi.org/10.1016/j.idcr.2014.10.010 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Case Report
Kapadia, Shashi
Patrawalla, Amee
Extrapulmonary tuberculosis presenting as a cavernous sinus syndrome: Case report with review of existing literature
title Extrapulmonary tuberculosis presenting as a cavernous sinus syndrome: Case report with review of existing literature
title_full Extrapulmonary tuberculosis presenting as a cavernous sinus syndrome: Case report with review of existing literature
title_fullStr Extrapulmonary tuberculosis presenting as a cavernous sinus syndrome: Case report with review of existing literature
title_full_unstemmed Extrapulmonary tuberculosis presenting as a cavernous sinus syndrome: Case report with review of existing literature
title_short Extrapulmonary tuberculosis presenting as a cavernous sinus syndrome: Case report with review of existing literature
title_sort extrapulmonary tuberculosis presenting as a cavernous sinus syndrome: case report with review of existing literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735080/
https://www.ncbi.nlm.nih.gov/pubmed/26839786
http://dx.doi.org/10.1016/j.idcr.2014.10.010
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