Mazouni Chafika, Girard Guillaume, Deter Russell, Haumonte Jean-Baptiste, Blanc Bernard, Bretelle Florence
Department of Obstetrics and Gynecology, Marseille Public Hospital System, Marseille, France.
Fertil Steril. 2008 Jan;89(1):219-22. doi: 10.1016/j.fertnstert.2007.02.044. Epub 2007 May 4.
To evaluate the circumstances associated with the diagnosis of Mullerian anomalies in adults.
Retrospective observational study.
University hospital.
PATIENT(S): All patients with Mullerian anomalies referred for evaluation.
INTERVENTION(S): All patients underwent radiologic and operative diagnostic workup using ultrasonography, or ultrasonography and hysteroscopy, and in some cases laparoscopy.
MAIN OUTCOME MEASURE(S): Clinical symptoms and radiologic investigations leading to the diagnosis. Mode and number of investigations before the diagnosis, and the time since the initial symptoms to the final diagnosis.
RESULT(S): One hundred ten patients were diagnosed with Mullerian anomalies: 73 septate uteri, 20 bicornuate uteri, 10 uterine hypoplasia, 4 unicornuate uteri, and 3 with Mayer- Mayer-Rokitansy-Küster-Hauser syndrome. The circumstances leading to the diagnosis were infertility (33.6%), repeat miscarriage (18.2%), ultrasonography during pregnancy (12.7%), pregnancy complications during last trimester (11%), abnormal examination (8.2%), and miscellaneous causes (16.3%). Up 50% of patients complained of gynecologic signs before the appropriate diagnosis. Radiologic diagnosis required two complementary imaging techniques in 62% of patients and more than two in 28%. The correct diagnosis was established in only 40% of cases before hospitalization. Most of the anomalies were initially diagnosed at hysterosalpingography and ultrasonography. The mean time between the first imaging examination and the diagnosis in a specialized department was 6.7 (+/-7.1) months.
CONCLUSION(S): The diagnosis of Mullerian anomalies in adults is often made at the time of conception and obstetric complications. There is a tendency toward the use of multiple imaging techniques and this delayed the diagnosis.
评估成年女性苗勒管异常诊断的相关情况。
回顾性观察研究。
大学医院。
所有因苗勒管异常前来评估的患者。
所有患者均接受了超声检查、超声联合宫腔镜检查,部分患者还接受了腹腔镜检查,以进行影像学和手术诊断评估。
导致诊断的临床症状和影像学检查。诊断前检查的方式和次数,以及从最初症状出现到最终诊断的时间。
110例患者被诊断为苗勒管异常:73例为纵隔子宫,20例为双角子宫,10例为子宫发育不全,4例为单角子宫,3例为 Mayer-Rokitansy-Küster-Hauser 综合征。导致诊断的情况包括不孕(33.6%)、反复流产(18.2%)、孕期超声检查(12.7%)、妊娠晚期并发症(11%)、检查异常(8.2%)以及其他原因(16.3%)。在正确诊断之前,高达50%的患者有妇科症状。62%的患者需要两种互补的影像学技术进行放射学诊断,28%的患者需要两种以上。住院前仅有40%的病例确诊。大多数异常最初在子宫输卵管造影和超声检查时被诊断。从首次影像学检查到专科诊断的平均时间为6.7(±7.1)个月。
成年女性苗勒管异常的诊断通常在受孕时和产科并发症时做出。存在使用多种影像学技术的趋势,这导致了诊断延迟。