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Actinomycotic osteomyelitis of a long bone in an immunocompetent adult: a case report and literature review
BACKGROUND: Actinomycosis is a rare, chronic granulomatous disease caused by Gram-positive anaerobic bacteria that colonize the oral cavity. Cervicofacial actinomycosis is the most frequent clinical presentation of actinomycosis, but hematogenous osteomyelitis at distant sites can occur in rare inst...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6495508/ https://www.ncbi.nlm.nih.gov/pubmed/31043170 http://dx.doi.org/10.1186/s12891-019-2576-2 |
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author | Ryu, Dong Jin Jeon, Yoon Sang Kwon, Hea Yoon Choi, Suk Jin Roh, Tae Hoon Kim, Myung Ku |
author_facet | Ryu, Dong Jin Jeon, Yoon Sang Kwon, Hea Yoon Choi, Suk Jin Roh, Tae Hoon Kim, Myung Ku |
author_sort | Ryu, Dong Jin |
collection | PubMed |
description | BACKGROUND: Actinomycosis is a rare, chronic granulomatous disease caused by Gram-positive anaerobic bacteria that colonize the oral cavity. Cervicofacial actinomycosis is the most frequent clinical presentation of actinomycosis, but hematogenous osteomyelitis at distant sites can occur in rare instance in immunocompromised or pediatric patients, only a few cases have been reported in healthy patients. Here we described a new case of distal femur osteomyelitis caused by Actinomyces in an adult patient who was immunocompetent and had no predisposing factors. CASE PRESENTATION: A woman aged 52 years with no history of trauma presented with severe pain, swelling, and increased local heat in the proximal area of the right knee 3 weeks after she first noticed discomfort. Magnetic resonance imaging showed persistent osteomyelitis of the distal metaphysis and diaphysis of the femur with a multifocal intraosseous abscess pocket. An incision and drainage of the abscess were conducted. The tissue culture, fungus culture, acid fast bacillus (AFB) culture, AFB smear, and tuberculosis polymerase chain reaction test results were negative. A pathologic examination confirmed the presence of actinomycosis. The patient was successfully treated with intravenous penicillin G for 8 weeks followed by oral amoxicillin-clavulanate for 6 weeks with repeated surgical debridement and drainage. After a 5-year follow up, the patient had no signs of recurring infection or complications and she had full range of movement in the affected knee. CONCLUSIONS: Although rare, actinomycotic osteomyelitis can occur in healthy people. Furthermore, actinomycotic osteomyelitis is easily misdiagnosed as tuberculosis in areas with a high prevalence of tuberculosis. To detect and identify the bacteria accurately, pathologic examination should be performed as well as culture tests, because the probability for culture confirmation of actinomycosis is quite low. The initial treatment is vital to a successful outcome without ostectomy or amputation. |
format | Online Article Text |
id | pubmed-6495508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64955082019-05-08 Actinomycotic osteomyelitis of a long bone in an immunocompetent adult: a case report and literature review Ryu, Dong Jin Jeon, Yoon Sang Kwon, Hea Yoon Choi, Suk Jin Roh, Tae Hoon Kim, Myung Ku BMC Musculoskelet Disord Case Report BACKGROUND: Actinomycosis is a rare, chronic granulomatous disease caused by Gram-positive anaerobic bacteria that colonize the oral cavity. Cervicofacial actinomycosis is the most frequent clinical presentation of actinomycosis, but hematogenous osteomyelitis at distant sites can occur in rare instance in immunocompromised or pediatric patients, only a few cases have been reported in healthy patients. Here we described a new case of distal femur osteomyelitis caused by Actinomyces in an adult patient who was immunocompetent and had no predisposing factors. CASE PRESENTATION: A woman aged 52 years with no history of trauma presented with severe pain, swelling, and increased local heat in the proximal area of the right knee 3 weeks after she first noticed discomfort. Magnetic resonance imaging showed persistent osteomyelitis of the distal metaphysis and diaphysis of the femur with a multifocal intraosseous abscess pocket. An incision and drainage of the abscess were conducted. The tissue culture, fungus culture, acid fast bacillus (AFB) culture, AFB smear, and tuberculosis polymerase chain reaction test results were negative. A pathologic examination confirmed the presence of actinomycosis. The patient was successfully treated with intravenous penicillin G for 8 weeks followed by oral amoxicillin-clavulanate for 6 weeks with repeated surgical debridement and drainage. After a 5-year follow up, the patient had no signs of recurring infection or complications and she had full range of movement in the affected knee. CONCLUSIONS: Although rare, actinomycotic osteomyelitis can occur in healthy people. Furthermore, actinomycotic osteomyelitis is easily misdiagnosed as tuberculosis in areas with a high prevalence of tuberculosis. To detect and identify the bacteria accurately, pathologic examination should be performed as well as culture tests, because the probability for culture confirmation of actinomycosis is quite low. The initial treatment is vital to a successful outcome without ostectomy or amputation. BioMed Central 2019-05-01 /pmc/articles/PMC6495508/ /pubmed/31043170 http://dx.doi.org/10.1186/s12891-019-2576-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Ryu, Dong Jin Jeon, Yoon Sang Kwon, Hea Yoon Choi, Suk Jin Roh, Tae Hoon Kim, Myung Ku Actinomycotic osteomyelitis of a long bone in an immunocompetent adult: a case report and literature review |
title | Actinomycotic osteomyelitis of a long bone in an immunocompetent adult: a case report and literature review |
title_full | Actinomycotic osteomyelitis of a long bone in an immunocompetent adult: a case report and literature review |
title_fullStr | Actinomycotic osteomyelitis of a long bone in an immunocompetent adult: a case report and literature review |
title_full_unstemmed | Actinomycotic osteomyelitis of a long bone in an immunocompetent adult: a case report and literature review |
title_short | Actinomycotic osteomyelitis of a long bone in an immunocompetent adult: a case report and literature review |
title_sort | actinomycotic osteomyelitis of a long bone in an immunocompetent adult: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6495508/ https://www.ncbi.nlm.nih.gov/pubmed/31043170 http://dx.doi.org/10.1186/s12891-019-2576-2 |
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