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Xanthogranulomatous Salpingitis Associated with a Large Uterine Leiomyoma
A case of xanthogranulomatous salpingitis (XGS) associated with a large uterine leiomyoma in a 50-year-old woman is presented. Xanthogranulomatous inflammation is an uncommon form of chronic inflammation that is destructive to affected organs. It is characterized by the presence of lipid-filled macr...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2963120/ https://www.ncbi.nlm.nih.gov/pubmed/20981281 http://dx.doi.org/10.1155/2010/970805 |
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author | Howey, Joanne Margaret Mahe, Etienne Radhi, Jasim |
author_facet | Howey, Joanne Margaret Mahe, Etienne Radhi, Jasim |
author_sort | Howey, Joanne Margaret |
collection | PubMed |
description | A case of xanthogranulomatous salpingitis (XGS) associated with a large uterine leiomyoma in a 50-year-old woman is presented. Xanthogranulomatous inflammation is an uncommon form of chronic inflammation that is destructive to affected organs. It is characterized by the presence of lipid-filled macrophages with admixed lymphocytes, plasma cells, and neutrophils. A review of the literature revealed that most patients with XGS have a clinical history of long-standing pelvic inflammatory disease (PID) or, less often, endometriosis. We report a case lacking a history of either PID or endometriosis but with a concurrent large uterine leiomyoma. Although the exact etiology in this case was not clear, the leiomyoma may have played a contributory role in pathogenesis. |
format | Text |
id | pubmed-2963120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-29631202010-10-27 Xanthogranulomatous Salpingitis Associated with a Large Uterine Leiomyoma Howey, Joanne Margaret Mahe, Etienne Radhi, Jasim Case Rep Med Case Report A case of xanthogranulomatous salpingitis (XGS) associated with a large uterine leiomyoma in a 50-year-old woman is presented. Xanthogranulomatous inflammation is an uncommon form of chronic inflammation that is destructive to affected organs. It is characterized by the presence of lipid-filled macrophages with admixed lymphocytes, plasma cells, and neutrophils. A review of the literature revealed that most patients with XGS have a clinical history of long-standing pelvic inflammatory disease (PID) or, less often, endometriosis. We report a case lacking a history of either PID or endometriosis but with a concurrent large uterine leiomyoma. Although the exact etiology in this case was not clear, the leiomyoma may have played a contributory role in pathogenesis. Hindawi Publishing Corporation 2010 2010-10-17 /pmc/articles/PMC2963120/ /pubmed/20981281 http://dx.doi.org/10.1155/2010/970805 Text en Copyright © 2010 Joanne Margaret Howey et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Howey, Joanne Margaret Mahe, Etienne Radhi, Jasim Xanthogranulomatous Salpingitis Associated with a Large Uterine Leiomyoma |
title | Xanthogranulomatous Salpingitis Associated with a Large Uterine Leiomyoma |
title_full | Xanthogranulomatous Salpingitis Associated with a Large Uterine Leiomyoma |
title_fullStr | Xanthogranulomatous Salpingitis Associated with a Large Uterine Leiomyoma |
title_full_unstemmed | Xanthogranulomatous Salpingitis Associated with a Large Uterine Leiomyoma |
title_short | Xanthogranulomatous Salpingitis Associated with a Large Uterine Leiomyoma |
title_sort | xanthogranulomatous salpingitis associated with a large uterine leiomyoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2963120/ https://www.ncbi.nlm.nih.gov/pubmed/20981281 http://dx.doi.org/10.1155/2010/970805 |
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