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原发性局限性膀胱淀粉样变性——一例病例报告并文献复习

Primary localised bladder amyloidosis - A case report with review of the literature.

作者信息

Yanada Brendan Akihiko, Soputro Nicolas Adrianto, Dias Brendan Hermenigildo

机构信息

Surgical Resident, Department of Urology, Western Health, Melbourne, Victoria, Australia.

Urology Fellow, Department of Urology, Western Health, Melbourne, Victoria, Australia.

出版信息

Urol Case Rep. 2022 Apr 2;43:102072. doi: 10.1016/j.eucr.2022.102072. eCollection 2022 Jul.

Abstract

Primary bladder amyloidosis, a mimicker of bladder malignancy, is a rare but important differential diagnosis for patients presenting with haematuria. We report the case of a 58-year-old man who initially presented with macroscopic haematuria and irritative urinary tract symptoms. There was no radiological evidence of a bladder mass lesion, but cystoscopy revealed an erythematous papillary lesion in the posterior bladder wall concerning for bladder malignancy. Histology demonstrated primary bladder amyloidosis, which was completely excised intraoperatively. He is undergoing regular cystoscopic surveillance and there has been no disease recurrence for 4 years since the initial diagnosis.

摘要

原发性膀胱淀粉样变性是膀胱恶性肿瘤的一种模仿者,对于出现血尿的患者来说,它是一种罕见但重要的鉴别诊断。我们报告一例58岁男性病例,该患者最初表现为肉眼血尿和刺激性尿路症状。影像学检查未发现膀胱肿块病变的证据,但膀胱镜检查发现膀胱后壁有一个红斑性乳头状病变,怀疑为膀胱恶性肿瘤。组织学检查显示为原发性膀胱淀粉样变性,术中已将其完全切除。他正在接受定期膀胱镜监测,自初次诊断以来4年未出现疾病复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cefa/8991461/ce3fa09c77f3/gr1.jpg

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