局限性尿道AL淀粉样变致尿道狭窄1例报告并文献复习。

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2025-08-05 eCollection Date: 2025-01-01 DOI:10.1159/000547759
Marialaina Carter, Samuel Hall, Rosetta Campbell, Omar Alkharabsheh, Nabin R Karki
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引用次数: 0

摘要

淀粉样蛋白原纤维在各个器官的沉积是淀粉样变性的一个标志,很少孤立于一个部位。我们报告一个23岁男性的局限性AL淀粉样变病例,他表现为尿道狭窄引起的血尿。尿道成形术中活检证实淀粉样蛋白沉积,液相色谱-质谱法鉴定AL亚型。病例介绍:全面检查,包括骨髓活检、脂肪垫活检、心脏检查和血清蛋白电泳,排除单克隆性疾病和广泛的淀粉样蛋白累及。患者接受了两期尿道成形术,随访期间没有局部或全身复发的迹象。结论:本病例强调了尿道淀粉样变在尿道狭窄的鉴别诊断、淀粉样变分型和排除全身累及的检查中的重要性。真正的局限性AL淀粉样变性最初不需要淀粉样蛋白定向治疗,但需要密切监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Urinary Stricture due to Localized Urethral AL Amyloidosis: A Case Report and Literature Review.

Introduction: The deposition of amyloid fibrils in various organs is a hallmark of amyloidosis, which is rarely isolated to a single site. We present a case of localized AL amyloidosis in a 23-year-old male who presented with hematuria from urethral stricture. Biopsy during urethroplasty confirmed amyloid deposition, and liquid chromatography-mass spectrometry identified the AL subtype.

Case presentation: A comprehensive workup, including bone marrow biopsy, fat pad biopsy, cardiac workup, and serum protein electrophoresis, excluded monoclonal disorder as well as widespread amyloid involvement. The patient underwent a two-stage urethroplasty and no evidence of recurrence locally or systemically during follow-up.

Conclusion: This case emphasizes the importance of considering urethral amyloidosis in the differential diagnosis of urethral strictures, amyloid typing, and workup to excluding systemic involvement. True localized AL amyloidosis does not need amyloid-directed therapy initially but warrants close monitoring.

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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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