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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...

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Autores principales: Mohamad, Abdur Rehman, Koleri, Junais, Hussain, Hussain Mohamed Sultan, Al Soub, Hussam, Al Maslamani, Muna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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.
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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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