A 30-year-old primiparous woman was referred to our perinatal center because of fetus growth restriction at 19 weeks of gestation with estimated fetal weight -1.8 SD, AFI 4.6 cm, and oligohydramnios. Fetal morphological assessment revealed normal findings, except for single umbilical artery. A karyotype of 46,XX was found at amniocentesis. During the course of pregnancy, fetal growth was estimated at between -1.8 and -2.0 SD, but the fetus was developing. The amount of amniotic fluid remained at 2 cm or more in the amniotic fluid pocket, and the Biophysical Profiling Score was 10 points. She visited our hospital because of decreased fetal movements at 37+4 weeks of gestation. The amniotic fluid index was less than 1 cm, and severe prolonged deceleration was observed. Thus, caesarean section was performed due to diagnosis of non-reassuring fetal status. A female infant weighing 2481 g (-0.55 SD) with 5/6 (1/5 min) Apgar score was delivered. Absence of peripheral malformation and a normal placenta were observed. The infant’s breathing state deteriorated after birth, and neonatal death due to respiratory failure resulted despite immediate intensive care. Autopsy revealed left hypoplastic lung and bilateral hypoplastic kidneys. After temporal oligohydramnios around 19 weeks of gestation, long-term oligohydramnios was not observed. The cause of death was not clinically determined, but the autopsy revealed renal hypoplasia and lung hypoplasia. Further, the alveoli were small and the septum was thick and immature. Even when temporal oligohydramnios occurs during early-mid gestation, this case suggests that lung immaturity can occur.
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