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Typical and atypical pelvic MRI characteristics of Mayer-Rokitansky-Kuster-Hauser syndrome: a comprehensive analysis of 201 patients

机译:Mayer-Rokitansky-Kuster-Hauser综合征的典型和非典型盆腔MRI特征:201例综合分析201例

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Objectives To comprehensively evaluate the pelvic magnetic resonance imaging (MRI) findings of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome and summarize the typical and atypical characteristics. Methods A retrospective analysis of 201 consecutive MRKH patients was carried out. Pelvic MRI was reviewed by two experienced gynecological radiologists in consensus. Characteristics including the morphology, signal pattern and volumes of the uterine rudiments, location and volume of the ovaries, and the degree of vaginal dysgenesis were evaluated. Other noted abnormalities were also recorded. Results Morphologically, the majority (95%) of patients displayed bilateral uterine rudiments combined with a fibrous band. The minority of patients showed no (3.5%) or unilateral (1.5%) uterine rudiments. A total of 385 uterine rudiments were detected which showed four types of signal patterns: one-layer differentiation (325, 84.4%), two-layer differentiation (27, 7%), three-layer differentiation without subsequent alteration (23, 6.0%), and three-layer differentiation with hematometra and/or ipsilateral hematosalpinx (10, 2.6%). The median volumes of these four types of uterine rudiments were 2.6 ml (1.69-3.81 ml), 3.19 ml (2.67-4.51 ml), 6.05 ml (3.37-12.44 ml), and 31.97 ml (19.2-38.7 ml), respectively. The mean ovarian volume was 6.49 +/- 3.91 ml. Abnormally located ovaries were detected in 63 (31.3%) patients. The distal vagina was discernable in 25.1% of patients. Conclusion MRKH patients typically display bilateral uterine rudiments combined with a fibrous band and normally located ovaries. The uterine rudiments are generally small with only one-layer differentiation, a subset of which might be large and exhibited other atypical presentations, including two- or three-layer differentiation or even hematometra. Abnormally located ovaries are not rare.
机译:目的以全面评估Mayer-Rokitansky-Kuster-Hauser(MRKH)综合征的盆腔磁共振成像(MRI)结果,并总结了典型和非典型特征。方法采用2011例患者对201连续MRTKH患者的回顾性分析。骨盆MRI被两名经验丰富的妇科放射科医师在共识中审查。评价包括卵巢窦,卵巢位置和体积的形态,信号模式和体积的特征,以及阴道膜缺陷程度。还记录了其他指出的异常。结果形态学上,大多数(95%)患者展示双侧子宫伴侣与纤维带相结合。少数患者没有(3.5%)或单侧(1.5%)子宫雏形。检测到总共385个子宫窦,其显示出四种类型的信号模式:单层分化(325,84.4%),双层分化(27,7%),三层分化而无需随后的变化(23,6.0% )和三层分化与血管物细胞和/或髂骨血液吡喃(10,2.6%)。这四种类型的子宫内侧的中值体积分别为2.6ml(1.69-3.81ml),3.19ml(2.67-4.51ml),6.05ml(3.37-12.44ml)和31.97ml(19.2-38.7ml)。平均卵巢体积为6.49 +/- 3.91毫升。在63例(31.3%)患者中检测到异常所在的卵巢。在25.1%的患者中,远端阴道可辨别。结论MRKH患者通常展示双侧子宫内侧,与纤维带和通常位于卵巢相结合。子宫窦通常仅具有单层分化,其子集可能大,并且表现出其他非典型呈现,包括两层或三层分化甚至血管瘤。异常所在的卵巢并不罕见。

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