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Double vagina and cervix communicating bilaterally with a single uterine cavity: report of a case with an unusual congenital uterine malformation.

机译:双阴道和子宫颈双侧与单个子宫腔进行双向通信:报告异常先天性子宫畸形的病例。

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BACKGROUND: The existence of a longitudinal vaginal septum with double cervix communicating bilaterally with a nonseptate uterine body and normal adnexa is an unusual mullerian anomaly. CASE: A 43-year-old woman presented with menorrhagia and duplication of the cervix and vagina. Afibromatous uterus was suggested by clinical examination and confirmed by ultrasonography. The patient underwent total abdominal hysterectomy with bilateral salpingooophorectomy. The surgical specimen revealed a fibromatous uterus with double cervix communicating bilaterally with a nonseptate uterine body; both adnexa were normal. CONCLUSION: This rare mullerian anomaly is inconsistent with the classical embryologic theory of caudal to cranial mullerian development but supports the alternative embryologic hypothesis suggested by Muller et al, according to which fusion and absorption begin at the isthmus and proceed simultaneously in both the cranial and caudal directions.
机译:背景:纵向阴道隔的存在是一个双子宫颈,与不分隔的子宫体和正常附件呈双侧连通,这是一种不常见的苗勒氏异常。病例:一名43岁妇女出现月经过多,子宫颈和阴道重复。临床检查提示纤维瘤性子宫,超声检查证实。该患者接受了全腹子宫切除术和双侧输卵管切除术。手术标本显示纤维状子宫,双子宫颈,双侧与不分隔的子宫体相通。附件都正常。结论:这种罕见的苗勒氏畸形与经典的从尾部到颅骨苗勒氏发育的胚胎学理论不一致,但支持Muller等人提出的另一种胚胎学假设,根据该假说,融合和吸收始于地峡,并在颅骨和尾鳍同时进行指示。

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