Imai A, Kawabata I, Tamaya T
Department of Obstetrics and Gynecology, Gifu University School of Medicine, Japan.
J Med. 1989;20(5-6):399-406.
A case of upper gastrointestinal dilatation associated with fluid collection in the peritoneal cavity is reported where the prenatal diagnosis was made sonographically in a non-immunologic hydrops fetalis. Neither generalized edema nor pleural effusion were detected. Polyhydramnios was complicated. Almost complete drainage of the abdominal fluid was accomplished with rapid re-accumulation of fetal ascites and no resolution of intestinal dilatation. After delivery by Cesarean section, the male infant died the next day due to respiratory distress syndrome. Postmortem histologic examination failed to confirm the ultrasonographic findings including ileal obstruction and subsequent hypoplasia in the colon. Despite the discrepancy between clinical and pathologic findings, the findings of this case would improve the etiology of hydrops where no possible cause is found.
本文报告一例上消化道扩张合并腹腔积液的病例,该病例在产前通过超声诊断为非免疫性胎儿水肿。未检测到全身性水肿或胸腔积液。并发羊水过多。几乎完全引流了腹腔积液,但胎儿腹水迅速重新积聚,肠道扩张未得到缓解。剖宫产分娩后,男婴因呼吸窘迫综合征于次日死亡。尸检组织学检查未能证实超声检查结果,包括回肠梗阻和随后的结肠发育不全。尽管临床和病理结果存在差异,但该病例的发现将有助于完善未发现可能病因的胎儿水肿的病因学。