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磁共振成像评估苗勒管发育异常女性的卵巢未降发生率。

Incidence of ovarian maldescent in women with mullerian duct anomalies: evaluation by MRI.

机构信息

Mallinckrodt Institute of Radiology, St. Louis, MO 63110, USA.

出版信息

AJR Am J Roentgenol. 2012 Apr;198(4):W381-5. doi: 10.2214/AJR.11.6595.

Abstract

OBJECTIVE

The objective of our study was to evaluate the incidence of ovarian mal-descent in patients with and in those without müllerian duct anomalies.

MATERIALS AND METHODS

Multiplanar MRI examinations of patients with (n = 65) and those without (n = 64) congenital uterine anomalies were evaluated for ovarian size, position, follicle count, and associated renal anomalies. Patients who were pregnant, had known prior pelvic surgery, or had large uterine leiomyomas were excluded. Two criteria were used to determine ovarian malposition: Was the upper pole of the ovary above the pelvic brim, as defined by the pubic symphysis-sacral promontory line, or was the upper pole of the ovary at or above the iliac artery bifurcation?

RESULTS

The müllerian duct anomalies identified in the study group included hypoplasia, unicornuate, didelphys, bicornuate, and septate uterus. Ovarian maldescent was identified in 12 of 65 women with uterine anomalies (17%) as compared with two of 64 women with normal uterine anatomy (3%) using the criterion of the ovarian pole being above the iliac bifurcation. Among the women with müllerian duct anomalies, only three of 29 with septate uterus (10%) had ovarian maldescent compared with the remaining nine of 36 women with other anomalies (25%). Ovarian size did not vary significantly between the two groups. Follicle count was increased in women with müllerian duct anomalies. Renal anomalies were present in 16 of 65 patients, five of whom had concomitant ovarian maldescent.

CONCLUSION

The incidence of ovarian maldescent is increased in patients with müllerian duct anomalies, with the highest association seen in those with didelphys, unicornuate, or bicornuate uterus.

摘要

目的

我们研究的目的是评估有和没有苗勒管畸形的患者卵巢位置异常的发生率。

材料与方法

对 65 例有先天性子宫畸形的患者(n = 65)和 64 例无先天性子宫畸形的患者(n = 64)的多平面 MRI 检查结果进行评估,评估内容包括卵巢大小、位置、卵泡计数和相关的肾脏异常。排除了妊娠、已知盆腔手术史或有较大的子宫平滑肌瘤的患者。使用两种标准来确定卵巢位置异常:卵巢上极是否高于耻骨联合-骶骨岬线定义的骨盆边缘,或者卵巢上极是否位于髂动脉分叉之上?

结果

在研究组中,苗勒管畸形包括发育不全、单角子宫、双子宫、双角子宫和纵隔子宫。使用卵巢极位于髂动脉分叉之上的标准,在 65 例有子宫畸形的患者中发现 12 例(17%)存在卵巢位置异常,而在 64 例子宫解剖正常的患者中发现 2 例(3%)。在有苗勒管畸形的患者中,只有 29 例纵隔子宫患者中有 3 例(10%)存在卵巢位置异常,而其余 36 例有其他畸形的患者中有 9 例(25%)存在卵巢位置异常。两组患者的卵巢大小无显著差异。苗勒管畸形患者的卵泡计数增加。65 例患者中有 16 例存在肾脏异常,其中 5 例同时存在卵巢位置异常。

结论

苗勒管畸形患者卵巢位置异常的发生率增加,双子宫、单角子宫或双角子宫畸形患者的相关性最高。

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