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Prenatal fetal peritoneal‑amniotic shunt combined with postnatal comprehensive conservative therapy for congenital chylous ascites: a case report

Published on Aug. 03, 2026Total Views: 40 times Total Downloads: 9 times Download Mobile

Author: FENG Qing 1 MO Yuxiao 1 WEI Cong 1 HE Bingyan 1 ZHAO Dongchi 1

Affiliation: 1.Department of Pediatrics, Women and Children's Hospital, Zhongnan Hospital of Wuhan University, Wuhan 430071, China

Keywords: Congenital chylous ascites Fetal peritoneal-amniotic shunt conservative therapy Total parenteral nutrition

DOI: 10.12173/j.issn.1004-4337.202603102

Reference: Feng Q, Mo YX, Wei C, et al. Prenatal fetal peritoneal‑amniotic shunt combined with postnatal comprehensive conservative therapy for congenital chylous ascites: a case report [J]. Journal of Mathematical Medicine, 2026, 39(7): 523-529. DOI: 10.12173/j.issn.1004-4337.202603102.[Article in Chinese]

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Abstract

Congenital chylous ascites (CCA) is a rare neonatal lymphatic disorder with an incidence of approximately 1/20,000 live births. It results from abnormal lymphatic development leading to chyle leakage into the peritoneal cavity, which may cause severe malnutrition, infection, and respiratory distress in fetuses and neonates. This article reports a case of fetal ascites detected by prenatal ultrasound screening and suspected as CCA after prenatal evaluation; a fetal peritoneal-amniotic shunt (PAS) was performed in the late gestational period as an intrauterine intervention. After birth, the diagnosis of CCA was confirmed, and individualized conservative treatment was initiated, including fasting, total parenteral nutrition, intermittent abdominal paracentesis with drainage, and continuous intravenous infusion of octreotide. During treatment, the infant's ascites volume, nutritional status, and liver and kidney function were dynamically monitored. The ascites gradually decreased, gastrointestinal function gradually recovered, and the infant was successfully transitioned to normal feeding before discharge. After discharge, the patient was readmitted due to recurrent ascites. Both octreotide and somatostatin administration induced drug-related cholestasis, which resolved after discontinuation. Regular follow-up with abdominal ultrasound at 2, 3, and 4 months of age showed small amounts of fluid that gradually decreased, with complete resolution by 6 months. At 9 months of age, the infant demonstrated good physical growth, normal motor, neurological, and cognitive development, and no signs of recurrent infection or immunodeficiency. This case suggests that an integrated management model characterized by "late‑gestation fetal PAS combined with early postnatal octreotide sequential therapy" can effectively control CCA, avoid surgical intervention, and achieve favorable long-term outcomes. Such reports are rare in the current literature, and this model provides a feasible clinical reference for the perinatal management of massive CCA.

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References

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