David M P, Fagot R
Geburtshilfe Frauenheilkd. 1977 Dec;37(12):1039-43.
A rare genital double malformation is dealt with in short. Including the four cases, which are reported, the number of the known cases in the literature amounts to only 31. The characteristic feature of the malformation is a communication of embryological origin between two uterine cavities. Diagnostic difficulties and clinical peculiarities can arise. Very often the genital malformation is accompanied by unilateral agenesis of kidney and ureter. Some clinical symptoms cannot be recognized and treated without knowledge about the existence of communication uteri, but the knowledge that malformations of the urinary tract may coexist is not less important. Indeed, it may be crucial for the patient's destiny.
简要介绍了一种罕见的生殖器双重畸形。包括所报道的4例病例，文献中已知病例数仅为31例。该畸形的特征是两个子宫腔之间存在胚胎学来源的交通。可能会出现诊断困难和临床特点。生殖器畸形常伴有单侧肾和输尿管发育不全。如果不了解子宫交通的存在，一些临床症状就无法被识别和治疗，但了解尿路畸形可能并存同样重要。事实上，这对患者的命运可能至关重要。
