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Bladder Malakoplakia in Systemic Sclerosis Patient: A Case Report and Review Literature
Malakoplakia, an anecdotal reactive granulomatous lesion, is a rare pathologic entity but relatively more common in genitourinary tracts. Here we report a case of malakoplakia in the urinary bladder in systemic sclerosis. The patient was a 66-year-old female treated with long-term corticosteroid and...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025697/ https://www.ncbi.nlm.nih.gov/pubmed/29967807 http://dx.doi.org/10.1089/cren.2018.0038 |
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author | Sirithanaphol, Wichien Sangkhamanon, Sakkarn Netwijitpan, Sittichai Foocharoen, Chingching |
author_facet | Sirithanaphol, Wichien Sangkhamanon, Sakkarn Netwijitpan, Sittichai Foocharoen, Chingching |
author_sort | Sirithanaphol, Wichien |
collection | PubMed |
description | Malakoplakia, an anecdotal reactive granulomatous lesion, is a rare pathologic entity but relatively more common in genitourinary tracts. Here we report a case of malakoplakia in the urinary bladder in systemic sclerosis. The patient was a 66-year-old female treated with long-term corticosteroid and cyclophosphamide. She presented with gross hematuria, and cystoscopy and biopsy revealed malakoplakia. There was no tumor and the stains for infectious organism were all negative. To the best of our knowledge, this is the first case report of malakoplakia in a systemic sclerosis patient. |
format | Online Article Text |
id | pubmed-6025697 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Mary Ann Liebert, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60256972018-07-02 Bladder Malakoplakia in Systemic Sclerosis Patient: A Case Report and Review Literature Sirithanaphol, Wichien Sangkhamanon, Sakkarn Netwijitpan, Sittichai Foocharoen, Chingching J Endourol Case Rep Case Report Malakoplakia, an anecdotal reactive granulomatous lesion, is a rare pathologic entity but relatively more common in genitourinary tracts. Here we report a case of malakoplakia in the urinary bladder in systemic sclerosis. The patient was a 66-year-old female treated with long-term corticosteroid and cyclophosphamide. She presented with gross hematuria, and cystoscopy and biopsy revealed malakoplakia. There was no tumor and the stains for infectious organism were all negative. To the best of our knowledge, this is the first case report of malakoplakia in a systemic sclerosis patient. Mary Ann Liebert, Inc. 2018-06-01 /pmc/articles/PMC6025697/ /pubmed/29967807 http://dx.doi.org/10.1089/cren.2018.0038 Text en © Wichien Sirithanaphol et al. 2018; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Sirithanaphol, Wichien Sangkhamanon, Sakkarn Netwijitpan, Sittichai Foocharoen, Chingching Bladder Malakoplakia in Systemic Sclerosis Patient: A Case Report and Review Literature |
title | Bladder Malakoplakia in Systemic Sclerosis Patient: A Case Report and Review Literature |
title_full | Bladder Malakoplakia in Systemic Sclerosis Patient: A Case Report and Review Literature |
title_fullStr | Bladder Malakoplakia in Systemic Sclerosis Patient: A Case Report and Review Literature |
title_full_unstemmed | Bladder Malakoplakia in Systemic Sclerosis Patient: A Case Report and Review Literature |
title_short | Bladder Malakoplakia in Systemic Sclerosis Patient: A Case Report and Review Literature |
title_sort | bladder malakoplakia in systemic sclerosis patient: a case report and review literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025697/ https://www.ncbi.nlm.nih.gov/pubmed/29967807 http://dx.doi.org/10.1089/cren.2018.0038 |
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