Abdominal Actinomycosis misdiagnosed as liposarcoma

ABSTRACT 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.

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Main Authors: Monteiro,Eunice Vieira e, Gaspar,Joana, Paiva,Claudia, Correia,Raquel, Valente,Vitor, Coelho,André, Lamas,Nuno Jorge
Format: Digital revista
Language:English
Published: Hospital Universitário da Universidade de São Paulo 2020
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2236-19602020000100604
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spelling oai:scielo:S2236-196020200001006042020-10-19Abdominal Actinomycosis misdiagnosed as liposarcomaMonteiro,Eunice Vieira eGaspar,JoanaPaiva,ClaudiaCorreia,RaquelValente,VitorCoelho,AndréLamas,Nuno Jorge Abdominal actinomycosis liposarcoma challenging diagnosis ABSTRACT 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.info:eu-repo/semantics/openAccessHospital Universitário da Universidade de São PauloAutopsy and Case Reports v.10 n.1 20202020-01-01info:eu-repo/semantics/reporttext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S2236-19602020000100604en10.4322/acr.2020.137
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country Brasil
countrycode BR
component Revista
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databasecode rev-scielo-br
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region America del Sur
libraryname SciELO
language English
format Digital
author Monteiro,Eunice Vieira e
Gaspar,Joana
Paiva,Claudia
Correia,Raquel
Valente,Vitor
Coelho,André
Lamas,Nuno Jorge
spellingShingle Monteiro,Eunice Vieira e
Gaspar,Joana
Paiva,Claudia
Correia,Raquel
Valente,Vitor
Coelho,André
Lamas,Nuno Jorge
Abdominal Actinomycosis misdiagnosed as liposarcoma
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
title Abdominal Actinomycosis misdiagnosed as liposarcoma
title_short 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_sort abdominal actinomycosis misdiagnosed as liposarcoma
description ABSTRACT 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.
publisher Hospital Universitário da Universidade de São Paulo
publishDate 2020
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S2236-19602020000100604
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