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本文引用的文献

1
Müllerianosis of the urinary bladder.膀胱苗勒管残余症
Int J Surg Pathol. 2011 Aug;19(4):548-51. doi: 10.1177/1066896911409578. Epub 2011 Jun 1.
2
Mullerianosis involving the urinary bladder.累及膀胱的苗勒管残余症
Int Urogynecol J. 2012 Jan;23(1):123-5. doi: 10.1007/s00192-011-1455-7. Epub 2011 May 27.
3
Mullerianosis of the urinary bladder: report of a case with diagnosis suggested in urine cytology and review of literature.膀胱苗勒管瘤病:1例尿液细胞学提示诊断的病例报告及文献复习
Diagn Cytopathol. 2012 Nov;40(11):997-1001. doi: 10.1002/dc.21693. Epub 2011 Apr 28.
4
Ureteral mullerianosis.输尿管苗勒管化生
J Endourol. 2009 Dec;23(12):1933-5. doi: 10.1089/end.2009.0321.
5
Endosalpingiosis of the urinary bladder: a case of probable implantative origin with characterization of benign Fallopian tube immunohistochemistry.膀胱子宫内膜异位症:一例可能起源于植入性的病例,并对良性输卵管进行免疫组织化学特征分析。
Int J Surg Pathol. 2010 Oct;18(5):381-3. doi: 10.1177/1066896909332730. Epub 2009 Mar 11.
6
Mullerianosis in post-caesarean section abdominal scar.
Indian J Pathol Microbiol. 2007 Jul;50(3):601-2.
7
Müllerianosis of ureter: a rare cause of hydronephrosis.输尿管苗勒管残余综合征:肾积水的罕见病因。
Urology. 2007 Jun;69(6):1208.e9-11. doi: 10.1016/j.urology.2007.03.012.
8
Endometrioid carcinoma of the urinary bladder complicating vesical Mullerianosis: a case report and review of the literature.膀胱子宫内膜样癌合并膀胱苗勒管化生:一例报告并文献复习
Virchows Arch. 2004 Jun;444(6):587-9. doi: 10.1007/s00428-004-1010-8. Epub 2004 Apr 23.
9
Mullerianosis of inguinal lymph nodes: report of a case.腹股沟淋巴结苗勒管瘤病:一例报告
Int J Gynecol Pathol. 2002 Jan;21(1):60-4. doi: 10.1097/00004347-200201000-00011.
10
Müllerianosis of the ureter: a metaplastic lesion.输尿管苗勒管化生:一种化生病变。
J Urol. 1999 Dec;162(6):2090-1. doi: 10.1016/S0022-5347(05)68111-6.

苗勒管瘤病:急性肾绞痛的罕见病因。

Mullerianosis: a rare cause of acute renal colic.

作者信息

Ndokera Rufaro, Brewster Simon, Dhar Sunanda

机构信息

Oxford Foundation School, Oxford, Oxon, UK.

出版信息

BMJ Case Rep. 2012 Oct 24;2012:bcr2012006704. doi: 10.1136/bcr-2012-006704.

DOI:10.1136/bcr-2012-006704
PMID:23097575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4544067/
Abstract

A 50-year-old woman presented to the urology department with an acute history suggestive of left-sided renal colic. There were no other associated symptoms, but urine dipstick revealed non-visible haematuria. CT-KUB revealed a soft tissue mass at the left vesico-ureteric junction. Flexible cystoscopy demonstrated a mass intruding into the posterior bladder. A transurethral resection of the bladder 'tumour' was undertaken, and it was noted that the mass was not macroscopically consistent with transitional cell carcinoma. Histology demonstrated Müllerianosis, a rare lesion characterised by locally invasive growth of tissue originating from the Müllerian (paramesonephric) duct. The patient was seen by gynaecologist who initiated hormone treatment with an lutenising hormone--releasing hormone (LH-RH) analogue. Urological follow-up 3 months later highlighted ongoing pelvic pain but no further colicky loin pain. Repeat cystoscopy showed the mass had become smaller and the left ureter was laterally displaced. Further gynaecological input is planned if symptoms are ongoing.

摘要

一名50岁女性因提示左侧肾绞痛的急性病史就诊于泌尿外科。无其他相关症状,但尿试纸检测显示镜下血尿。CT-KUB检查显示左膀胱输尿管连接处有一软组织肿块。软性膀胱镜检查发现有一肿块突入膀胱后部。进行了经尿道膀胱“肿瘤”切除术,发现该肿块在肉眼下与移行细胞癌不符。组织学检查显示为苗勒管腺病,这是一种罕见病变,其特征为源自苗勒(副中肾)管的组织呈局部浸润性生长。妇科医生对该患者进行了诊治,并开始使用促黄体生成素释放激素(LH-RH)类似物进行激素治疗。3个月后的泌尿外科随访显示仍有盆腔疼痛,但未再出现肾绞痛。重复膀胱镜检查显示肿块变小,左侧输尿管向外侧移位。如果症状持续,计划进一步寻求妇科方面的建议。