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Abdominopelvic Actinomycosis Mimicking Peritoneal Carcinomatosis: A Case Report

Actinomycosis is a rare chronic bacterial infection primarily caused by Actinomyces israelii. A 47-year-old woman presented to our clinic with a 1-week history of lower abdominal pain. Preoperative imaging studies revealed multiple peritoneal and pelvic masses suggestive of malignancy. The primary t...

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Autores principales: Kim, Sungjin, Kang, Sung Il, Kim, Sohyun, Jang, Min Hye, Kim, Jae Hwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Coloproctology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837399/
https://www.ncbi.nlm.nih.gov/pubmed/32054258
http://dx.doi.org/10.3393/ac.2019.11.07
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author Kim, Sungjin
Kang, Sung Il
Kim, Sohyun
Jang, Min Hye
Kim, Jae Hwang
author_facet Kim, Sungjin
Kang, Sung Il
Kim, Sohyun
Jang, Min Hye
Kim, Jae Hwang
author_sort Kim, Sungjin
collection PubMed
description Actinomycosis is a rare chronic bacterial infection primarily caused by Actinomyces israelii. A 47-year-old woman presented to our clinic with a 1-week history of lower abdominal pain. Preoperative imaging studies revealed multiple peritoneal and pelvic masses suggestive of malignancy. The primary tumor could not be identified despite further endoscopic and gynecological evaluation. On exploration for tissue confirmation, excisional biopsies from multiple masses were performed because complete excision was not possible. Histopathological examination confirmed actinomycosis with multiple abscesses, and the patient was treated with antibiotics. We present a case of disseminated peritoneal actinomycosis that mimicked malignant peritoneal carcinomatosis on imaging studies.
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spelling pubmed-78373992021-02-02 Abdominopelvic Actinomycosis Mimicking Peritoneal Carcinomatosis: A Case Report Kim, Sungjin Kang, Sung Il Kim, Sohyun Jang, Min Hye Kim, Jae Hwang Ann Coloproctol Case Report Actinomycosis is a rare chronic bacterial infection primarily caused by Actinomyces israelii. A 47-year-old woman presented to our clinic with a 1-week history of lower abdominal pain. Preoperative imaging studies revealed multiple peritoneal and pelvic masses suggestive of malignancy. The primary tumor could not be identified despite further endoscopic and gynecological evaluation. On exploration for tissue confirmation, excisional biopsies from multiple masses were performed because complete excision was not possible. Histopathological examination confirmed actinomycosis with multiple abscesses, and the patient was treated with antibiotics. We present a case of disseminated peritoneal actinomycosis that mimicked malignant peritoneal carcinomatosis on imaging studies. Korean Society of Coloproctology 2020-12 2019-11-13 /pmc/articles/PMC7837399/ /pubmed/32054258 http://dx.doi.org/10.3393/ac.2019.11.07 Text en Copyright © 2020 The Korean Society of Coloproctology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kim, Sungjin
Kang, Sung Il
Kim, Sohyun
Jang, Min Hye
Kim, Jae Hwang
Abdominopelvic Actinomycosis Mimicking Peritoneal Carcinomatosis: A Case Report
title Abdominopelvic Actinomycosis Mimicking Peritoneal Carcinomatosis: A Case Report
title_full Abdominopelvic Actinomycosis Mimicking Peritoneal Carcinomatosis: A Case Report
title_fullStr Abdominopelvic Actinomycosis Mimicking Peritoneal Carcinomatosis: A Case Report
title_full_unstemmed Abdominopelvic Actinomycosis Mimicking Peritoneal Carcinomatosis: A Case Report
title_short Abdominopelvic Actinomycosis Mimicking Peritoneal Carcinomatosis: A Case Report
title_sort abdominopelvic actinomycosis mimicking peritoneal carcinomatosis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837399/
https://www.ncbi.nlm.nih.gov/pubmed/32054258
http://dx.doi.org/10.3393/ac.2019.11.07
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