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Rebellious headache revealing an extensive rhinoscleroma: A case report and review of the literature
and importance: this case report aimed at an unusual case of extensive rhinoscleroma with a literature review, We report this case to bring attention to the patients with immunodeficiency problem regardless of presenting symptoms. Case presentation: a 70 -year-old patient with diabetes and hypertens...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893451/ https://www.ncbi.nlm.nih.gov/pubmed/33643651 http://dx.doi.org/10.1016/j.amsu.2021.02.012 |
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author | Bazzout, Asmae Lachkar, Azzeddine Benfadil, Drissia Tsen, Adil abdenbi El ayoubi, Fahd Ghailan, Rachid |
author_facet | Bazzout, Asmae Lachkar, Azzeddine Benfadil, Drissia Tsen, Adil abdenbi El ayoubi, Fahd Ghailan, Rachid |
author_sort | Bazzout, Asmae |
collection | PubMed |
description | and importance: this case report aimed at an unusual case of extensive rhinoscleroma with a literature review, We report this case to bring attention to the patients with immunodeficiency problem regardless of presenting symptoms. Case presentation: a 70 -year-old patient with diabetes and hypertension, consulted for chronic median and posterior headaches have not improved with symptomatic treatment. She reported cacosmia without rhinorrhea and right otalgia. The examination of the nasal cavity showed a bleeding lesion on the lateral wall of the nasopharynx. CT-scan of the facial showed tissue lesion on the posterior and lateral walls of the nasopharynx, with infiltration of the parapharyngeal space and bone lysis right edge of the clivus. The biopsy confirmed the diagnosis of rhinoscleroma. The patient started the ciprofloxacin for 3 months, and the evolvement has noticed with the disappearance of the lesion during the first month of treatment. The patient started the ciprofloxacin for 3 months, and the evolvement was noticed with the disappearance of the lesion during the first month of treatment. Cilinical discussion: rhinoscleroma is a chronic and progressive granulomatous disease of the nasal cavities. The diagnosis is confirmed by the search for bacteria and an anatomopathological assessment of MIKULICZ cells. The medical treatment of choice has a high concentration in macrophages such as rifampicin and fluoroquinolone. Conclusion: rhinoscleroma is a granulomatous disease caused by klebsiella rhinoscleromatis, you must think about in front a nasopharyngeal lesion imitating a malignant pathology. |
format | Online Article Text |
id | pubmed-7893451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-78934512021-02-25 Rebellious headache revealing an extensive rhinoscleroma: A case report and review of the literature Bazzout, Asmae Lachkar, Azzeddine Benfadil, Drissia Tsen, Adil abdenbi El ayoubi, Fahd Ghailan, Rachid Ann Med Surg (Lond) Case Report and importance: this case report aimed at an unusual case of extensive rhinoscleroma with a literature review, We report this case to bring attention to the patients with immunodeficiency problem regardless of presenting symptoms. Case presentation: a 70 -year-old patient with diabetes and hypertension, consulted for chronic median and posterior headaches have not improved with symptomatic treatment. She reported cacosmia without rhinorrhea and right otalgia. The examination of the nasal cavity showed a bleeding lesion on the lateral wall of the nasopharynx. CT-scan of the facial showed tissue lesion on the posterior and lateral walls of the nasopharynx, with infiltration of the parapharyngeal space and bone lysis right edge of the clivus. The biopsy confirmed the diagnosis of rhinoscleroma. The patient started the ciprofloxacin for 3 months, and the evolvement has noticed with the disappearance of the lesion during the first month of treatment. The patient started the ciprofloxacin for 3 months, and the evolvement was noticed with the disappearance of the lesion during the first month of treatment. Cilinical discussion: rhinoscleroma is a chronic and progressive granulomatous disease of the nasal cavities. The diagnosis is confirmed by the search for bacteria and an anatomopathological assessment of MIKULICZ cells. The medical treatment of choice has a high concentration in macrophages such as rifampicin and fluoroquinolone. Conclusion: rhinoscleroma is a granulomatous disease caused by klebsiella rhinoscleromatis, you must think about in front a nasopharyngeal lesion imitating a malignant pathology. Elsevier 2021-02-10 /pmc/articles/PMC7893451/ /pubmed/33643651 http://dx.doi.org/10.1016/j.amsu.2021.02.012 Text en © 2021 The Authors http://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 Bazzout, Asmae Lachkar, Azzeddine Benfadil, Drissia Tsen, Adil abdenbi El ayoubi, Fahd Ghailan, Rachid Rebellious headache revealing an extensive rhinoscleroma: A case report and review of the literature |
title | Rebellious headache revealing an extensive rhinoscleroma: A case report and review of the literature |
title_full | Rebellious headache revealing an extensive rhinoscleroma: A case report and review of the literature |
title_fullStr | Rebellious headache revealing an extensive rhinoscleroma: A case report and review of the literature |
title_full_unstemmed | Rebellious headache revealing an extensive rhinoscleroma: A case report and review of the literature |
title_short | Rebellious headache revealing an extensive rhinoscleroma: A case report and review of the literature |
title_sort | rebellious headache revealing an extensive rhinoscleroma: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893451/ https://www.ncbi.nlm.nih.gov/pubmed/33643651 http://dx.doi.org/10.1016/j.amsu.2021.02.012 |
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