Stanimir Marius, ChiuŢu LuminiŢa Cristina, Wese Sébastien, Milulescu Amelia, Nemeş Răducu Nicolae, Bratu Ovidiu Gabriel
Department of Anesthesiology and Intensive Care, University of Medicine and Pharmacy of Craiova, Romania;
Rom J Morphol Embryol. 2016;57(2 Suppl):849-852.
The aim of this paper is to report a very rare case of müllerianosis (endosalpinx, endometrium, and endocervix) in a post-menopausal woman. Müllerianosis of the bladder is a very rare disease, which affects mainly the women of the reproductive age group, but with a good prognosis if the transitional bladder carcinoma is resolved. We present the case of a 64-year-old woman complaining of left lower abdomen pain, repeated lower and upper tract urinary infections, emergency urinary incontinence and hematuria. The surgical history shows that she underwent a hysterectomy, caesarean section and appendectomy. The clinical examination emphasizes a normal abdomen, with a normal aspect of the post-operative scars and a second-degree cystocele. An abdominal computed tomography (CT) scan with contrast and a cystography were performed and showed a 16 mm lesion-like tumor on the left bladder wall respectively a third-degree vesicoureteral reflux. These investigations were followed by a cystoscopy and transurethral resection of the bladder tumor (TURBT). The histopathology report described three types of tissues: endometriosis, endocervicosis and endosalpingiosis. Sequent to these results, a partial cystectomy with the re-implantation of the left ureter was performed. Once again, the results of the specimen confirm the diagnosis of müllerianosis. The immediate post-operative outcomes were good, the patient having no pains and no more hematuria. Six month later, a tension-free vaginal tape obturator (TVT-O) operation was carried out for urinary incontinence and two years later, a correction for a post-surgical abdominal hernia was performed. Müllerianosis of the bladder is a very rare disease, which affects mainly the women at the procreation age, but with a good prognosis. The differential diagnosis with a malignant tumor is very important to be carefully made. Currently, there is no golden standard to treat this disease. The cystoscopy and the histopathological examination of the specimen are indispensable for the certainty diagnosis.
本文旨在报告一名绝经后女性极为罕见的苗勒管化生病例(输卵管内膜、子宫内膜和宫颈内膜)。膀胱苗勒管化生是一种非常罕见的疾病,主要影响育龄期女性,但如果能解决移行性膀胱癌问题,则预后良好。我们呈现了一名64岁女性的病例,她主诉左下腹疼痛、反复的下尿路和上尿路感染、急迫性尿失禁和血尿。手术史显示她接受过子宫切除术、剖宫产术和阑尾切除术。临床检查显示腹部正常,术后瘢痕外观正常,存在二度膀胱膨出。进行了腹部增强计算机断层扫描(CT)和膀胱造影,分别显示左膀胱壁有一个16毫米的类肿瘤病变以及三度膀胱输尿管反流。这些检查之后进行了膀胱镜检查和经尿道膀胱肿瘤切除术(TURBT)。组织病理学报告描述了三种组织类型:子宫内膜异位、宫颈内膜异位和输卵管内膜异位。基于这些结果,进行了部分膀胱切除术并重新植入左输尿管。标本结果再次证实了苗勒管化生的诊断。术后即刻效果良好,患者无疼痛且不再有血尿。六个月后,因尿失禁进行了无张力阴道吊带闭孔术(TVT - O),两年后,对术后腹部疝进行了修复。膀胱苗勒管化生是一种非常罕见的疾病,主要影响生育年龄的女性,但预后良好。与恶性肿瘤的鉴别诊断非常重要,必须仔细进行。目前,治疗这种疾病尚无金标准。膀胱镜检查和标本的组织病理学检查对于明确诊断必不可少。