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Septate uterus with a double cervix and longitudinal vaginal septum.

机译:子宫分隔,具双子宫颈和阴道纵隔。

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摘要

OBJECTIVE: To report the clinical features of 9 cases and review the previously reported 8 cases of an uncommon mullerian anomaly, characterized by the presence of a complete uterine septum with cervical duplication and represent a a longitudinal vaginal septum. STUDY DESIGN: Retrospective clinical study. RESULTS: Nine patients aged 21-32 presented to our clinic with complaints of dyspareunia, dysmenorrhea, and primary or secondary infertility. All 9 patients displayed a single uterus with smooth fundal contour, double cervix and longitudinal vaginal septum. Some additional abnormal findings were associated with these anomalies in some patients: polycystic ovaries in 3 cases and different degrees of endometriosis in 2 cases. Most of the patients had normal tubal patency. CONCLUSION: According to a MEDLINE search, only 8 cases of septate uterus with cervical duplication and a longitudinal vaginal septum have been reported to date. We report 9 more cases, which suggest that this atypical septate uterus type is probably more frequent than reported. These cases support the bidirectional mullerian theory and may imply the presence of another type of mullerian anomaly.
机译:目的:报告9例的临床特点,并回顾先前报道的8例罕见的苗勒氏畸形,其特征是存在完整的子宫间隔并带有宫颈重复,并代表纵向阴道间隔。研究设计:回顾性临床研究。结果:9例21-32岁的患者因痛经,痛经以及原发性或继发性不孕症出现在我们诊所。所有9例患者均表现为子宫单个,子宫底轮廓光滑,双子宫颈和阴道纵隔。在某些患者中,与这些异常相关的其他一些异常发现:多囊卵巢3例,不同程度的子宫内膜异位2例。大多数患者的输卵管通畅性正常。结论:根据MEDLINE搜索,迄今仅报告了8例具有子宫颈复制和纵向阴道中隔的分隔子宫。我们报告了9例,这表明这种非典型的分隔子宫类型可能比所报道的更为频繁。这些情况支持双向米勒理论,并可能暗示存在另一种类型的米勒异常。

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