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Cervical spondylodiscitis caused by Candida albicans in a non-immunocompromised patient: A case report and review of literature
BACKGROUND: Fungal cervical spondylodiscitis is rare and accounts for less than 1% of all cervical, thoracic, and lumbar vertebral osteomyelitis and discitis. CASE DESCRIPTION: A 32-year-old non-immunocompromised male presented with persistent neck pain and paresthesias. The magnetic resonance imagi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744757/ https://www.ncbi.nlm.nih.gov/pubmed/31528486 http://dx.doi.org/10.25259/SNI_240_2019 |
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author | Huang, Shiwei Kappel, Ari D. Peterson, Catherine Chamiraju, Parthasarathi Rajah, Gary B. Moisi, Marc D. |
author_facet | Huang, Shiwei Kappel, Ari D. Peterson, Catherine Chamiraju, Parthasarathi Rajah, Gary B. Moisi, Marc D. |
author_sort | Huang, Shiwei |
collection | PubMed |
description | BACKGROUND: Fungal cervical spondylodiscitis is rare and accounts for less than 1% of all cervical, thoracic, and lumbar vertebral osteomyelitis and discitis. CASE DESCRIPTION: A 32-year-old non-immunocompromised male presented with persistent neck pain and paresthesias. The magnetic resonance imaging of the cervical spine demonstrated a contrast-enhancing erosive lesion involving the cervical C6 and C7 vertebral bodies accompanied by epidural phlegmon. Blood culture was negative. The patient underwent a C6 and C7 anterior corpectomy with instrumented fusion (e.g., expandable cage C5 to T1). Intraoperatively, frank pus was noted within the C6-C7 disc space and was accompanied by thick prevertebral and epidural phlegmon extending from C5 to T1. Intraoperative cultures grew Candida albicans. Three days later, a C6-C7 laminectomy with C4-T2 posterior instrumented fusion was performed; the cultures again grew C. albicans. The patient was treated with intravenous micafungin for 14 days followed by 6–12 months of 400 mg oral fluconazole daily. CONCLUSION: There are few cases in literature where non-immunocompromised patients developed fungal cervical spondylodiscitis. Prompt diagnosis and appropriate management are critical to effectively treat these patients. Surgical intervention may warrant corpectomy, discectomy, and operative debridement followed by long-term targeted antifungal therapy. |
format | Online Article Text |
id | pubmed-6744757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-67447572019-09-16 Cervical spondylodiscitis caused by Candida albicans in a non-immunocompromised patient: A case report and review of literature Huang, Shiwei Kappel, Ari D. Peterson, Catherine Chamiraju, Parthasarathi Rajah, Gary B. Moisi, Marc D. Surg Neurol Int Case Report BACKGROUND: Fungal cervical spondylodiscitis is rare and accounts for less than 1% of all cervical, thoracic, and lumbar vertebral osteomyelitis and discitis. CASE DESCRIPTION: A 32-year-old non-immunocompromised male presented with persistent neck pain and paresthesias. The magnetic resonance imaging of the cervical spine demonstrated a contrast-enhancing erosive lesion involving the cervical C6 and C7 vertebral bodies accompanied by epidural phlegmon. Blood culture was negative. The patient underwent a C6 and C7 anterior corpectomy with instrumented fusion (e.g., expandable cage C5 to T1). Intraoperatively, frank pus was noted within the C6-C7 disc space and was accompanied by thick prevertebral and epidural phlegmon extending from C5 to T1. Intraoperative cultures grew Candida albicans. Three days later, a C6-C7 laminectomy with C4-T2 posterior instrumented fusion was performed; the cultures again grew C. albicans. The patient was treated with intravenous micafungin for 14 days followed by 6–12 months of 400 mg oral fluconazole daily. CONCLUSION: There are few cases in literature where non-immunocompromised patients developed fungal cervical spondylodiscitis. Prompt diagnosis and appropriate management are critical to effectively treat these patients. Surgical intervention may warrant corpectomy, discectomy, and operative debridement followed by long-term targeted antifungal therapy. Scientific Scholar 2019-08-02 /pmc/articles/PMC6744757/ /pubmed/31528486 http://dx.doi.org/10.25259/SNI_240_2019 Text en Copyright: © 2019 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Huang, Shiwei Kappel, Ari D. Peterson, Catherine Chamiraju, Parthasarathi Rajah, Gary B. Moisi, Marc D. Cervical spondylodiscitis caused by Candida albicans in a non-immunocompromised patient: A case report and review of literature |
title | Cervical spondylodiscitis caused by Candida albicans in a non-immunocompromised patient: A case report and review of literature |
title_full | Cervical spondylodiscitis caused by Candida albicans in a non-immunocompromised patient: A case report and review of literature |
title_fullStr | Cervical spondylodiscitis caused by Candida albicans in a non-immunocompromised patient: A case report and review of literature |
title_full_unstemmed | Cervical spondylodiscitis caused by Candida albicans in a non-immunocompromised patient: A case report and review of literature |
title_short | Cervical spondylodiscitis caused by Candida albicans in a non-immunocompromised patient: A case report and review of literature |
title_sort | cervical spondylodiscitis caused by candida albicans in a non-immunocompromised patient: a case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744757/ https://www.ncbi.nlm.nih.gov/pubmed/31528486 http://dx.doi.org/10.25259/SNI_240_2019 |
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