Gupta I, Barson A J
J Clin Pathol. 1980 Jul;33(7):679-83. doi: 10.1136/jcp.33.7.679.
Two cases of hydrocolpos are described presenting soon after birth. One infant who died on the first day had an intrauterine peritonitis caused by compression of the caecum on the pelvic brim. The other surviving infant developed a caecal perforation secondary to Hirschsprung's disease. Neither infant had rectal atresia, which is the commonest cause of intestinal obstruction in these infants. The association of hydrocolpos with polydactyly in one of these cases may represent an autosomal recessive trait.
本文描述了两例出生后不久即出现的阴道积水病例。其中一名在出生第一天死亡的婴儿因盲肠在骨盆边缘受压导致宫内腹膜炎。另一名存活的婴儿继发于先天性巨结肠病出现盲肠穿孔。两名婴儿均无直肠闭锁,而直肠闭锁是这些婴儿肠梗阻最常见的原因。其中一例阴道积水与多指畸形相关,可能代表一种常染色体隐性性状。