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Head and neck tuberculosis associated to sarcoidosis: A case report

The distinction between tuberculosis and sarcoidosis presents sometimes a clinical challenge. Their sequential occurrence in the same patient is uncommon. We present the case of a 42-year-old female with a proven diagnosis of tuberculous lymphadenitis who has developed successively nasal tuberculosi...

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Autores principales: Mediouni, Azza, Najjar, Sabrine, Boukriba, Seif, Chelly, Baya, Chahed, Houda, Besbes, Ghazi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130336/
https://www.ncbi.nlm.nih.gov/pubmed/37122614
http://dx.doi.org/10.1016/j.jctube.2023.100364
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author Mediouni, Azza
Najjar, Sabrine
Boukriba, Seif
Chelly, Baya
Chahed, Houda
Besbes, Ghazi
author_facet Mediouni, Azza
Najjar, Sabrine
Boukriba, Seif
Chelly, Baya
Chahed, Houda
Besbes, Ghazi
author_sort Mediouni, Azza
collection PubMed
description The distinction between tuberculosis and sarcoidosis presents sometimes a clinical challenge. Their sequential occurrence in the same patient is uncommon. We present the case of a 42-year-old female with a proven diagnosis of tuberculous lymphadenitis who has developed successively nasal tuberculosis and pulmonary sarcoidosis respectively after 10 and 14 months of antituberculosis treatment. The patient presented with bilateral cervical lymphadenopathy. Tuberculin skin test was negative. Chest radiography was normal. An excision biopsy was taken and histopathological examination established tuberculosis diagnosis. Therapy with antituberculosis drugs was started, and cervical lymphadenopathy showed progressive resolution. Subsequently, nearly 10 months after, the patient developed new cervical lymphadenopathies and nasal obstruction. Tuberculosis of the nasal mucosa was confirmed by biopsy. Antituberclosis bitherapy was enhanced by ofloxacin and ethambutol. Thoracic CT scan showed several nodular elements in both lungs, with bilateral enlarged mediastinal adenopathy. Bronchoalveolar lavage showed a lymphocytic alveolitis with a CD4/CD8 ratio of 5, consistent with the diagnosis of pulmonary sarcoidosis. Corticosteroid treatment, in form of oral prednisolone was introduced, 3 months after sarcoidosis diagnosis have been setteled; because of pulmonary fibrosis noticed on thoracic CT. Systemic corticotherapy was continued for a further period of 3 years, until all the lesions cleared out. The present case emphasizes the possible association between tuberculosis and sarcoidosis.
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spelling pubmed-101303362023-04-27 Head and neck tuberculosis associated to sarcoidosis: A case report Mediouni, Azza Najjar, Sabrine Boukriba, Seif Chelly, Baya Chahed, Houda Besbes, Ghazi J Clin Tuberc Other Mycobact Dis Case Report The distinction between tuberculosis and sarcoidosis presents sometimes a clinical challenge. Their sequential occurrence in the same patient is uncommon. We present the case of a 42-year-old female with a proven diagnosis of tuberculous lymphadenitis who has developed successively nasal tuberculosis and pulmonary sarcoidosis respectively after 10 and 14 months of antituberculosis treatment. The patient presented with bilateral cervical lymphadenopathy. Tuberculin skin test was negative. Chest radiography was normal. An excision biopsy was taken and histopathological examination established tuberculosis diagnosis. Therapy with antituberculosis drugs was started, and cervical lymphadenopathy showed progressive resolution. Subsequently, nearly 10 months after, the patient developed new cervical lymphadenopathies and nasal obstruction. Tuberculosis of the nasal mucosa was confirmed by biopsy. Antituberclosis bitherapy was enhanced by ofloxacin and ethambutol. Thoracic CT scan showed several nodular elements in both lungs, with bilateral enlarged mediastinal adenopathy. Bronchoalveolar lavage showed a lymphocytic alveolitis with a CD4/CD8 ratio of 5, consistent with the diagnosis of pulmonary sarcoidosis. Corticosteroid treatment, in form of oral prednisolone was introduced, 3 months after sarcoidosis diagnosis have been setteled; because of pulmonary fibrosis noticed on thoracic CT. Systemic corticotherapy was continued for a further period of 3 years, until all the lesions cleared out. The present case emphasizes the possible association between tuberculosis and sarcoidosis. Elsevier 2023-04-03 /pmc/articles/PMC10130336/ /pubmed/37122614 http://dx.doi.org/10.1016/j.jctube.2023.100364 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Mediouni, Azza
Najjar, Sabrine
Boukriba, Seif
Chelly, Baya
Chahed, Houda
Besbes, Ghazi
Head and neck tuberculosis associated to sarcoidosis: A case report
title Head and neck tuberculosis associated to sarcoidosis: A case report
title_full Head and neck tuberculosis associated to sarcoidosis: A case report
title_fullStr Head and neck tuberculosis associated to sarcoidosis: A case report
title_full_unstemmed Head and neck tuberculosis associated to sarcoidosis: A case report
title_short Head and neck tuberculosis associated to sarcoidosis: A case report
title_sort head and neck tuberculosis associated to sarcoidosis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130336/
https://www.ncbi.nlm.nih.gov/pubmed/37122614
http://dx.doi.org/10.1016/j.jctube.2023.100364
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