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Granulomatous prostatitis: clinical and histomorphologic survey of the disease in a tertiary care hospital

机译:肉芽肿性前列腺炎:三级医院对该疾病的临床和组织形态学调查

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Background Granulomatous prostatitis is an uncommon entity that is diagnosed incidentally on histopathology and is broadly classified as nonspecific, specific, postsurgical (post-transurethral resection), or secondary to other rare systemic granulomatous diseases. Only very few studies are available in the literature that describe the clinical and histomorphological spectrum of the disease. Methods A retrospective analysis of histopathological records of 1,181 prostatic specimens received in the pathology department was done over a period of 13 years (January 2003 to January 2016). All histologically proven cases of granulomatous prostatitis were retrieved, and relevant clinical data were collected from patients’ records. Epstein and Hutchins classification was used to categorize these cases. Results Twenty-two cases of granulomatous prostatitis were identified, accounting for an incidence of 1.86%. Among these, nonspecific granulomatous prostatitis ( n = 10) was the most common followed by tubercular prostatitis ( n = 5), posttransurethral resection of the prostate ( n = 3), allergic ( n = 2), and xanthogranulomatous prostatitis ( n = 2). The age range of these patients was between 41 and 75 years, with the majority of patients in their 7 th decade. Serum prostate-specific antigen levels ranged between 0.88?ng/mL and 19.22?ng/mL. Hard and fixed nodules were observed on digital rectal examination in 14 cases. Transrectal ultrasound revealed hypoechoic shadows in five cases. Conclusion Despite present-day advances in imaging modalities and serological investigations, it is virtually impossible to identify granulomatous prostatitis clinically. Histopathology remains the gold standard in diagnosing the disease. However, assigning an etiologic cause to the wide spectrum of granulomas in granulomatous prostatitis requires a pathologist’s expertise and proper clinical correlation for appropriate patient management.
机译:背景肉芽肿性前列腺炎是一种罕见的实体,在组织病理学上被偶然诊断,大致分为非特异性,特异性,外科手术后(经尿道切除)或继发于其他罕见的系统性肉芽肿性疾病。在描述该疾病的临床和组织形态谱的文献中只有很少的研究可用。方法回顾性分析在13年(2003年1月至2016年1月)中病理科接受的1181份前列腺标本的组织病理学记录。所有组织学证实的肉芽肿性前列腺炎病例均被检索,并从患者记录中收集了相关的临床数据。使用爱泼斯坦和哈钦斯分类法对这些病例进行分类。结果确定肉芽肿性前列腺炎22例,占1.86%。其中,非特异性肉芽肿性前列腺炎(n = 10)是最常见的,其次是结核性前列腺炎(n = 5),经尿道前列腺切除术(n = 3),变应性(n = 2)和黄皮肉芽肿性前列腺炎(n = 2)。 )。这些患者的年龄范围在41至75岁之间,大多数患者在第7个十年中。血清前列腺特异性抗原水平介于0.88?ng / mL和19.22?ng / mL之间。直肠指检发现硬结节和固定节14例。经直肠超声检查发现5例出现低回声阴影。结论尽管目前在影像学方法和血清学研究方面已有进展,但实际上不可能在临床上鉴定肉芽肿性前列腺炎。组织病理学仍然是诊断该疾病的金标准。但是,要为肉芽肿性前列腺炎中的各种肉芽肿确定病因,就需要病理学家的专业知识和适当的临床相关性,以进行适当的患者管理。

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