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Abdominal Actinomycosis misdiagnosed as liposarcoma
Actinomycosis is an uncommon, endogenous, and chronic infection with varied and nonspecific clinical features such as abdominal, pelvic or cervical masses, ulcerative lesions, abscesses, draining fistula, fibrosis, and constitutional symptoms. The disease ensues when the bacteria disrupt the mucosal...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
São Paulo, SP: Universidade de São Paulo, Hospital Universitário
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945302/ https://www.ncbi.nlm.nih.gov/pubmed/32039066 http://dx.doi.org/10.4322/acr.2020.137 |
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author | Monteiro, Eunice Vieira e Gaspar, Joana Paiva, Claudia Correia, Raquel Valente, Vitor Coelho, André Lamas, Nuno Jorge |
author_facet | Monteiro, Eunice Vieira e Gaspar, Joana Paiva, Claudia Correia, Raquel Valente, Vitor Coelho, André Lamas, Nuno Jorge |
author_sort | Monteiro, Eunice Vieira e |
collection | PubMed |
description | Actinomycosis is an uncommon, endogenous, and chronic infection with varied and nonspecific clinical features such as abdominal, pelvic or cervical masses, ulcerative lesions, abscesses, draining fistula, fibrosis, and constitutional symptoms. The disease ensues when the bacteria disrupt the mucosal barrier, invade, and spread throughout interfascial planes. Currently, the diagnosis of actinomycosis is challenging because of its very low frequency and depending on the clinical presentation it may masquerade malignancies. Therapy consists initially in intravenous penicillin, followed by an oral regimen that may be extended until a year of treatment. A timely diagnosis is crucial to avoid extensive therapeutic attempt as surgery. However, a biopsy or drainage of abscesses and fistula’s tract may be required not only as a diagnostic procedure as part of the therapy. We report the case of a 72-year-old woman with an abdominal mass initially misdiagnosed as a liposarcoma. A second biopsy of a skin lesion of the abdominal wall made the diagnosis of actinomycosis, avoiding a major surgical procedure. The patient was treated with a long-term course of antibiotics with favorable outcome. Liposarcoma was ruled out after the patient’s full recovery with antibiotics and the misdiagnosis was credit to the overconfidence on the immunohistochemical positivity to MDM2. |
format | Online Article Text |
id | pubmed-6945302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | São Paulo, SP: Universidade de São Paulo, Hospital Universitário |
record_format | MEDLINE/PubMed |
spelling | pubmed-69453022020-02-07 Abdominal Actinomycosis misdiagnosed as liposarcoma Monteiro, Eunice Vieira e Gaspar, Joana Paiva, Claudia Correia, Raquel Valente, Vitor Coelho, André Lamas, Nuno Jorge Autops Case Rep Article / Clinical Case Report Actinomycosis is an uncommon, endogenous, and chronic infection with varied and nonspecific clinical features such as abdominal, pelvic or cervical masses, ulcerative lesions, abscesses, draining fistula, fibrosis, and constitutional symptoms. The disease ensues when the bacteria disrupt the mucosal barrier, invade, and spread throughout interfascial planes. Currently, the diagnosis of actinomycosis is challenging because of its very low frequency and depending on the clinical presentation it may masquerade malignancies. Therapy consists initially in intravenous penicillin, followed by an oral regimen that may be extended until a year of treatment. A timely diagnosis is crucial to avoid extensive therapeutic attempt as surgery. However, a biopsy or drainage of abscesses and fistula’s tract may be required not only as a diagnostic procedure as part of the therapy. We report the case of a 72-year-old woman with an abdominal mass initially misdiagnosed as a liposarcoma. A second biopsy of a skin lesion of the abdominal wall made the diagnosis of actinomycosis, avoiding a major surgical procedure. The patient was treated with a long-term course of antibiotics with favorable outcome. Liposarcoma was ruled out after the patient’s full recovery with antibiotics and the misdiagnosis was credit to the overconfidence on the immunohistochemical positivity to MDM2. São Paulo, SP: Universidade de São Paulo, Hospital Universitário 2019-12-13 /pmc/articles/PMC6945302/ /pubmed/32039066 http://dx.doi.org/10.4322/acr.2020.137 Text en Autopsy and Case Reports. ISSN 2236-1960. Copyright © 2020. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the article is properly cited. |
spellingShingle | Article / Clinical Case Report Monteiro, Eunice Vieira e Gaspar, Joana Paiva, Claudia Correia, Raquel Valente, Vitor Coelho, André Lamas, Nuno Jorge Abdominal Actinomycosis misdiagnosed as liposarcoma |
title | Abdominal Actinomycosis misdiagnosed as liposarcoma |
title_full | Abdominal Actinomycosis misdiagnosed as liposarcoma |
title_fullStr | Abdominal Actinomycosis misdiagnosed as liposarcoma |
title_full_unstemmed | Abdominal Actinomycosis misdiagnosed as liposarcoma |
title_short | Abdominal Actinomycosis misdiagnosed as liposarcoma |
title_sort | abdominal actinomycosis misdiagnosed as liposarcoma |
topic | Article / Clinical Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945302/ https://www.ncbi.nlm.nih.gov/pubmed/32039066 http://dx.doi.org/10.4322/acr.2020.137 |
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