输尿管狭窄由骨骼外软骨瘤:一个异常罕见的病例报告

IF 0.4 Q4 UROLOGY & NEPHROLOGY
Toshimitsu Tohya , Hiroshi Ishizaki , Yoshiki Futakuchi , Hideyuki Fukui , Kazutaka Ozono , Munekage Yamaguchi
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引用次数: 0

摘要

我们报告一个异常罕见的病例输尿管狭窄引起的骨骼外软骨瘤。一名60多岁的妇女因推测子宫肌瘤扭转而行腹腔镜子宫切除术,但后来出现严重的右侧疼痛。影像显示肾积水及输尿管狭窄,怀疑肿瘤。输尿管镜检查和活检证实了软骨瘤,这是1973年以来世界范围内报告的第二例病例。患者已接受定期输尿管支架置换治疗,导致症状缓解和肾积水改善。本病例强调了输尿管软骨瘤的极端罕见性,鉴别其与恶性肿瘤的诊断挑战,以及组织病理学证实的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ureteral stenosis due to extraskeletal chondroma: An exceptionally rare case report
We report an exceptionally rare case of ureteral stenosis caused by an extraskeletal chondroma. A woman in her 60s underwent laparoscopic hysterectomy for presumed uterine fibroid torsion, but later developed severe right flank pain. Imaging revealed hydronephrosis and ureteral stricture suspicious for tumor. Ureteroscopy with biopsy confirmed chondroma, representing only the second reported case worldwide after 1973. The patient has been managed with periodic ureteral stent exchanges, leading to symptom relief and improved hydronephrosis. This case highlights the extreme rarity of ureteral chondroma, the diagnostic challenge of differentiating it from malignancy, and the importance of histopathological confirmation.
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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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