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Eosinophilic cystitis complicated with cystitis glandularis: a case report

BACKGROUND: Eosinophilic cystitis (EC) is a rare inflammatory disease characterized by the gathering and infiltration of numerous eosinophilia (EOS) in the bladder wall. Because of Few cases of EC have been reported globally, the epidemiology of EC is not well known. We report herein the details of...

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Autores principales: Ye, Jun Bing, Chen, Qian, Zeng, Ke, Li, Xiao Bin, Deng, Ke Fei, Huang, Jun, Chen, Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8994907/
https://www.ncbi.nlm.nih.gov/pubmed/35397579
http://dx.doi.org/10.1186/s12894-022-01007-6
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author Ye, Jun Bing
Chen, Qian
Zeng, Ke
Li, Xiao Bin
Deng, Ke Fei
Huang, Jun
Chen, Rong
author_facet Ye, Jun Bing
Chen, Qian
Zeng, Ke
Li, Xiao Bin
Deng, Ke Fei
Huang, Jun
Chen, Rong
author_sort Ye, Jun Bing
collection PubMed
description BACKGROUND: Eosinophilic cystitis (EC) is a rare inflammatory disease characterized by the gathering and infiltration of numerous eosinophilia (EOS) in the bladder wall. Because of Few cases of EC have been reported globally, the epidemiology of EC is not well known. We report herein the details of one very scarce case of large tumor-like eosinophilic cystitis complicated with cystitis glandularis (CG) diagnosed by biopsy. CASE PRESENTATION: A 45-year-old Chinese man was referred to our hospital for the treatment of right lumbago and odynuria. Ultrasound examination indicated the low echo on the right portion wall and the neck of the bladder. Computed tomography showed a remarkable enhancing large mass that measured 5.0 cm × 2.3 cm located on the right portion of the bladder with undefined margin. For further treatment, diagnostic transurethral resection of the bladder was performed, the postoperative histopathological diagnosis was EC complicated with CG. After transurethral resection, antibiotics, glucocorticoids, and antihistamines were treated. The patient recovered uneventfully and was discharged on postoperative day 8 without evidence of recurrence followed-up for 6 months. CONCLUSION: Large tumor-like eosinophilic cystitis complicated with cystitis glandularis is rare, malignant tumors need to be ruled out. We deem that prompt biopsy led to the exact diagnosis, appropriate treatment led to better prognosis.
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spelling pubmed-89949072022-04-11 Eosinophilic cystitis complicated with cystitis glandularis: a case report Ye, Jun Bing Chen, Qian Zeng, Ke Li, Xiao Bin Deng, Ke Fei Huang, Jun Chen, Rong BMC Urol Case Report BACKGROUND: Eosinophilic cystitis (EC) is a rare inflammatory disease characterized by the gathering and infiltration of numerous eosinophilia (EOS) in the bladder wall. Because of Few cases of EC have been reported globally, the epidemiology of EC is not well known. We report herein the details of one very scarce case of large tumor-like eosinophilic cystitis complicated with cystitis glandularis (CG) diagnosed by biopsy. CASE PRESENTATION: A 45-year-old Chinese man was referred to our hospital for the treatment of right lumbago and odynuria. Ultrasound examination indicated the low echo on the right portion wall and the neck of the bladder. Computed tomography showed a remarkable enhancing large mass that measured 5.0 cm × 2.3 cm located on the right portion of the bladder with undefined margin. For further treatment, diagnostic transurethral resection of the bladder was performed, the postoperative histopathological diagnosis was EC complicated with CG. After transurethral resection, antibiotics, glucocorticoids, and antihistamines were treated. The patient recovered uneventfully and was discharged on postoperative day 8 without evidence of recurrence followed-up for 6 months. CONCLUSION: Large tumor-like eosinophilic cystitis complicated with cystitis glandularis is rare, malignant tumors need to be ruled out. We deem that prompt biopsy led to the exact diagnosis, appropriate treatment led to better prognosis. BioMed Central 2022-04-09 /pmc/articles/PMC8994907/ /pubmed/35397579 http://dx.doi.org/10.1186/s12894-022-01007-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Ye, Jun Bing
Chen, Qian
Zeng, Ke
Li, Xiao Bin
Deng, Ke Fei
Huang, Jun
Chen, Rong
Eosinophilic cystitis complicated with cystitis glandularis: a case report
title Eosinophilic cystitis complicated with cystitis glandularis: a case report
title_full Eosinophilic cystitis complicated with cystitis glandularis: a case report
title_fullStr Eosinophilic cystitis complicated with cystitis glandularis: a case report
title_full_unstemmed Eosinophilic cystitis complicated with cystitis glandularis: a case report
title_short Eosinophilic cystitis complicated with cystitis glandularis: a case report
title_sort eosinophilic cystitis complicated with cystitis glandularis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8994907/
https://www.ncbi.nlm.nih.gov/pubmed/35397579
http://dx.doi.org/10.1186/s12894-022-01007-6
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