Surgical management of complex atypical endometrial hyperplasia in a woman with rare genitourinary anomalies: unicornuate uterus with rudimentary horn, ipsilateral ectopic ovary and pelvic kidney

被引:1
|
作者
Grigoriadis, C. [1 ,2 ]
Tympa, A. [3 ]
Terzakis, E. [2 ]
Theodoraki, K. [3 ]
Hassiakos, D. [1 ,2 ]
机构
[1] Univ Athens, Aretaie Hosp, Dept Obstet & Gynecol 2, Athens, Greece
[2] Leto Matern Hosp, Athens, Greece
[3] Univ Athens, Aretaie Hosp, Dept Anesthesiol 1, Athens, Greece
来源
GIORNALE DI CHIRURGIA | 2018年 / 39卷 / 04期
关键词
Endometrial hyperplasia; Unicornuate uterus; Rudimentary horn; Ectopic ovary; Pelvic kidney;
D O I
10.11138/gchir/2018.39.4.245
中图分类号
R61 [外科手术学];
学科分类号
摘要
Aim. According to the so far published literature, only one case of endometrial cancer in a patient with unicornuate uterus has been reported. This is a case report study, presenting a rare case of complex atypical endometrial hyperplasia in a woman with unicornuate uterus and multiple genitourinary anomalies. Case report. A 43-year old G1P1 woman presented with episodes of menometrorrhagia and anemia. She had previous surgical history of laparoscopy due to infertility, in which she was diagnosed with unicornuate uterus with a rudimentary left uterine horn and ipsilateral ectopic ovary in the anatomic place of the left kidney. Dilatation and curettage was performed. Histology showed complex atypical endometrial hyperplasia. The patient underwent total abdominal hysterectomy with bilateral salpingo-oophorectomy, in an extremely interesting operation due to the multiple genitourinary anomalies. The uterus with a 6-centimeter uterine myoma and the adnexae were removed en block. Great effort was put into dissecting the left fallopian tube which arised from the cervix and via the rudimentary horn led to the left ectopic ovary that was located at the left kidneys' anatomic space. The patient recovered well and final histology was negative for malignancy. Discussion. All necessary imaging examinations have to be scheduled prior to surgical intervention in order to give valuable anatomic information in cases of women diagnosed with Mullerian abnormalities.
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页码:245 / 247
页数:3
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