Farber M, Mitchell G W
Am J Obstet Gynecol. 1979 Aug 15;134(8):881-4. doi: 10.1016/0002-9378(79)90861-5.
Partial atresia of the fallopian tube was discovered in two patients with double uteri of the bicornuate variety. The abnormal tube in each case was ipsilateral to a noncommunicating, nonfunctioning, rudimentary uterine horn. A normal fimbriated end led to a short, patent ampullary portion that ended blindly in the mesosalpinx. Realization of the potential for the coexistence of congenital malformation of the fallopian tubes with various uterine malformations suggests that extreme caution be exercised during adnexal surgery in patients with anomalous development of the müllerian ducts.
在两名双子宫双角子宫患者中发现了输卵管部分闭锁。在每例中，异常的输卵管与一个不连通、无功能的残角子宫同侧。正常的伞端通向一个短的、通畅的壶腹部，该壶腹部在输卵管系膜内盲端终止。认识到输卵管先天性畸形与各种子宫畸形共存的可能性，提示在苗勒管发育异常的患者进行附件手术时应格外谨慎。
