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Recurrent skull vault actinomycosis: A case report and review of literature
Actinomycosis is an uncommon cause of central nervous system infection. A case of skull bone osteomyelitis with epidural empyema is presented. A 44-year-old man presented with chronic osteomyelitis of skull vault with epidural and subgaleal collection diagnosed by histopathology as actinomycosis. He...
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/PMC8267539/ https://www.ncbi.nlm.nih.gov/pubmed/34277352 http://dx.doi.org/10.1016/j.idcr.2021.e01215 |
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author | Mohamad, Abdur Rehman Koleri, Junais Hussain, Hussain Mohamed Sultan Al Soub, Hussam Al Maslamani, Muna |
author_facet | Mohamad, Abdur Rehman Koleri, Junais Hussain, Hussain Mohamed Sultan Al Soub, Hussam Al Maslamani, Muna |
author_sort | Mohamad, Abdur Rehman |
collection | PubMed |
description | Actinomycosis is an uncommon cause of central nervous system infection. A case of skull bone osteomyelitis with epidural empyema is presented. A 44-year-old man presented with chronic osteomyelitis of skull vault with epidural and subgaleal collection diagnosed by histopathology as actinomycosis. He had similar lesion at the same site 10 years ago, which was excised completely. Recurrent Actinomycosis of the skull vault is uncommon in literature. This case highlights the importance of considering actinomycosis as a differential diagnosis of tumorous growths and stresses on the importance of tissue histopathology for diagnosis and need for surgery to control the disease. Treatment is prolonged, therefore compliance with the long-term antibiotic duration is essential to prevent complications and avoid recurrence. |
format | Online Article Text |
id | pubmed-8267539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-82675392021-07-16 Recurrent skull vault actinomycosis: A case report and review of literature Mohamad, Abdur Rehman Koleri, Junais Hussain, Hussain Mohamed Sultan Al Soub, Hussam Al Maslamani, Muna IDCases Case Report Actinomycosis is an uncommon cause of central nervous system infection. A case of skull bone osteomyelitis with epidural empyema is presented. A 44-year-old man presented with chronic osteomyelitis of skull vault with epidural and subgaleal collection diagnosed by histopathology as actinomycosis. He had similar lesion at the same site 10 years ago, which was excised completely. Recurrent Actinomycosis of the skull vault is uncommon in literature. This case highlights the importance of considering actinomycosis as a differential diagnosis of tumorous growths and stresses on the importance of tissue histopathology for diagnosis and need for surgery to control the disease. Treatment is prolonged, therefore compliance with the long-term antibiotic duration is essential to prevent complications and avoid recurrence. Elsevier 2021-07-03 /pmc/articles/PMC8267539/ /pubmed/34277352 http://dx.doi.org/10.1016/j.idcr.2021.e01215 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Mohamad, Abdur Rehman Koleri, Junais Hussain, Hussain Mohamed Sultan Al Soub, Hussam Al Maslamani, Muna Recurrent skull vault actinomycosis: A case report and review of literature |
title | Recurrent skull vault actinomycosis: A case report and review of literature |
title_full | Recurrent skull vault actinomycosis: A case report and review of literature |
title_fullStr | Recurrent skull vault actinomycosis: A case report and review of literature |
title_full_unstemmed | Recurrent skull vault actinomycosis: A case report and review of literature |
title_short | Recurrent skull vault actinomycosis: A case report and review of literature |
title_sort | recurrent skull vault actinomycosis: a case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267539/ https://www.ncbi.nlm.nih.gov/pubmed/34277352 http://dx.doi.org/10.1016/j.idcr.2021.e01215 |
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