[Large colpohematometra with bilateral hematosalpinx resulting from progressive obstruction caused by incomplete vaginal septum].

L Belvisi, F Bombelli, C Belloni, G L Taccagni
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Abstract

Complete or incomplete transverse vaginal septum is a rare malformation of the female genital tract. Usually the complete congenital type occurs at puberty because of the collection of menstrual blood above the septum with amenorrhea and cyclic lower abdominal pain as presenting symptoms. On the contrary, in the case shown by the authors, the subacute epilogue occurred in the perimenopausal phase: a very large colpohematometra is reported in a 49 years old woman, with an incomplete vaginal septum resulting in progressive obstruction. The association between this malformation and the presence of endometriotic localizations in the genital tract, as reported by other authors, is interesting. In this case, endometriosis can be secondary to the presence of the septum or could have determined the impairment of the obstruction in consequence of the associated status of chronic flogosis.

[由于阴道间隔不完全引起的进行性梗阻导致的大阴道积血伴双侧输卵管积血]。
完整或不完整的阴道横隔是一种罕见的女性生殖道畸形。完全先天性型通常发生在青春期,因为经血在间隔上方聚集,以闭经和周期性下腹部疼痛为主要症状。相反,在作者所显示的病例中,亚急性尾声发生在围绝经期:据报道,一名49岁妇女出现了非常大的阴道血肿,阴道间隔不完整导致进行性梗阻。据其他作者报道,这种畸形与生殖道子宫内膜异位症之间的联系是有趣的。在这种情况下,子宫内膜异位症可能继发于隔膜的存在,或者可能已经确定了慢性海绵畸形相关状态下梗阻的损害。
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