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低位直肠癌括约肌间切除术中遇到的完全性单侧输尿管重复畸形。

Complete unilateral ureteral duplication encountered during intersphincteric resection for low rectal cancer.

作者信息

Varlatzidou Alexandra, Zarokosta Maria, Nikou Euthumios, Theodoropoulos Panagiotis, Kakaviatos Dimosthenis, Piperos Τheodoros, Kalles Vasileios, Bonatsos Vasileios, Mariolis-Sapsakos Theodoros

机构信息

University Department of Surgery, General and Oncologic Hospital of Kifissia ''Agii Anargiri', Athens, Greece.

Anatomy and Histology Laboratory, School of Nursing, University of Athens, Greece.

出版信息

J Surg Case Rep. 2018 Oct 11;2018(10):rjy266. doi: 10.1093/jscr/rjy266. eCollection 2018 Oct.

DOI:10.1093/jscr/rjy266
PMID:30323916
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6180614/
Abstract

Complete duplication of ureters is a very rare clinical entity that may either be asymptomatic or present with a variety of clinical findings. In the presented case a 51-year-old Caucasian female underwent an intersphincteric resection for low rectal cancer. Intraoperatively, during the standard bilateral recognition and mobilization of the ureters, complete unilateral duplication of the left ureter was incidentally detected, deriving from a single renal parenchyma. Such a congenital abnormality though constitutes a major risk-factor of accidental ureteral injury during operations including pelvis. Conclusively, meticulous exposure of both ureters combined with surgeons' unceasing awareness constitute the cornerstone of a safe operation.

摘要

双侧输尿管完全重复是一种非常罕见的临床情况,可能无症状,也可能伴有多种临床表现。在本病例中,一名51岁的白种女性因低位直肠癌接受了括约肌间切除术。术中,在标准的双侧输尿管识别和游离过程中,偶然发现左侧输尿管完全单侧重复,起源于单一肾实质。尽管这种先天性异常是包括盆腔手术在内的手术中输尿管意外损伤的主要危险因素。总之,仔细暴露双侧输尿管并结合外科医生的持续警惕是安全手术的基石。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e759/6180614/05c7e76ebfc6/rjy266f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e759/6180614/8ebab574c770/rjy266f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e759/6180614/e763e7ecc14e/rjy266f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e759/6180614/1eaa91886428/rjy266f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e759/6180614/05c7e76ebfc6/rjy266f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e759/6180614/8ebab574c770/rjy266f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e759/6180614/e763e7ecc14e/rjy266f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e759/6180614/1eaa91886428/rjy266f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e759/6180614/05c7e76ebfc6/rjy266f04.jpg

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Int J Surg Case Rep. 2015;6C:23-5. doi: 10.1016/j.ijscr.2014.11.049. Epub 2014 Nov 20.
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A 52-year-old male with bilaterally duplicated collecting systems with obstructing ureteral stones: a case report.一名52岁男性,双侧重复肾盂集合系统合并输尿管梗阻性结石:病例报告。
Curr Urol. 2013 Nov;7(2):104-6. doi: 10.1159/000356257. Epub 2013 Oct 30.
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Unilateral complete ureteral duplication with distal ureteral stone: A rare entity.
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