Hendren W H, Oesch I L, Tschaeppeler H, Bettex M C
Z Kinderchir. 1987 Apr;42(2):115-9. doi: 10.1055/s-2008-1075565.
Cloacal malformations in female infants are not very common and their treatment is most challenging because every case differs from the others. In the light of a well-documented case, the authors describe the complexity of the malformation, the difficulties of making a correct detailed diagnosis, and the chronology of repair. They stress the advantage of the posterior sagittal approach for the first part of the operation, changing for the second part to a supine and later to a lithotomy position. In most cases a satisfactory reconstruction is possible, anatomically as well as functionally.
女性婴儿泄殖腔畸形并不常见，而且由于每个病例都各不相同，其治疗极具挑战性。根据一个记录详尽的病例，作者描述了该畸形的复杂性、做出正确详细诊断的困难以及修复的时间顺序。他们强调了后矢状入路在手术第一阶段的优势，第二阶段改为仰卧位，之后再改为截石位。在大多数情况下，无论在解剖学还是功能方面，都有可能实现令人满意的重建。
