Xanthogranulomatous prostatitis: benign prostate infection masquerading as invasive prostate cancer on MRI and PET-PSMA.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Kenneth Keen Yip Chew, Brianna Thompson, Mahtab Farzin, Eddy Lee Hao Wong
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引用次数: 0

Abstract

Xanthogranulomatous prostatitis (XGP) is a rare inflammatory condition that can closely mimic prostate adenocarcinoma both clinically and radiologically. We report the case of a man in his mid-60s who presented with pelvic discomfort, dysuria, reduced urine flow and fever. He had an elevated prostate-specific antigen (PSA) level of 17.5 ng/mL and abnormal findings on digital rectal examination. Multi-parametric MRI of the prostate revealed a prostate lesion suspicious for malignancy invading the rectal wall and right obturator internus muscle. However, transperineal prostate biopsies confirmed XGP with no evidence of cancer. The patient was treated with a 4-month course of ciprofloxacin, which resolved most of his symptoms, and alpha-blocker therapy was commenced to improve urine flow. This case emphasises the diagnostic challenges posed by XGP, which can mimic T4 prostate cancer and potentially lead to overtreatment. Awareness of this condition, along with systematic diagnostic strategies, is essential to avoid unnecessary interventions and optimise patient management.

黄色肉芽肿性前列腺炎:在MRI和PET-PSMA上伪装成侵袭性前列腺癌的良性前列腺感染。
摘要黄色肉芽肿性前列腺炎(XGP)是一种罕见的炎症性疾病,在临床和影像学上都与前列腺腺癌非常相似。我们报告的情况下,一名男子在他的60中期谁提出盆腔不适,排尿困难,减少尿流和发烧。前列腺特异性抗原(PSA)水平升高17.5 ng/mL,直肠指检异常。前列腺多参数MRI显示一前列腺病变疑似恶性侵犯直肠壁及右闭孔内肌。然而,经会阴前列腺活检证实XGP没有癌症的证据。患者接受了4个月的环丙沙星治疗,大部分症状得以缓解,并开始了α受体阻滞剂治疗以改善尿流。这个病例强调了XGP带来的诊断挑战,它可以模拟T4前列腺癌,并可能导致过度治疗。对这种情况的认识,以及系统的诊断策略,对于避免不必要的干预和优化患者管理至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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