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CASE REPORT article

Front. Pediatr.

Sec. Pediatric Surgery

This article is part of the Research TopicAdvances in Etiology Research and Clinical Intervention Strategies for Congenital Intestinal Malformations in ChildrenView all 8 articles

Case Report: Pediatric chylous ascites beyond congenital malformations - Infectious causes and nutritional management with a literature review

Provisionally accepted
Teresa  CapriatiTeresa Capriati1*Annalisa  CarciofiAnnalisa Carciofi1,2Chiara  GrimaldiChiara Grimaldi3Andrzej  KrzysztofiakAndrzej Krzysztofiak4Simona  GattiSimona Gatti2Maria  Elena LionettiMaria Elena Lionetti2Michela  CaprarelliMichela Caprarelli1Annalisa  MorelliAnnalisa Morelli1Lucia  TulliLucia Tulli1Antonella  DiamantiAntonella Diamanti1
  • 1Digestive Diseases and Nutritional Rehabilitation, "Bambino Gesù" Children's Hospital, IRCCS, Rome, Italy
  • 2Department of Pediatrics, Polytechnic University of Marche, 60123 Ancona, Italy
  • 3Surgical Oncology Unit, Bambino Gesù Pediatric Hospital IRCCS, Piazza S. Onofrio, Rome, Italy
  • 4Infectious Diseases Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy

The final, formatted version of the article will be published soon.

Chylous ascites (CA) is a condition characterized by the accumulation of lymphatic fluid in the peritoneal cavity. Although congenital malformations are the most common cause in newborns, infectious agents represent a clinically significant, potentially reversible etiology that benefits from specific therapy. Various pathogens, including bacteria, viruses, fungi, and parasites, can alter the lymphatic system and lead to the leakage of chyle into the peritoneal cavity, resulting in nutritional, immunological, and metabolic deficiencies. We describe the case of a 5-month-old infant presenting with acute abdomen (vomiting, irritability, and abdominal distension) associated with elevated lipase levels. He underwent emergency laparotomy, which revealed chylous ascites in the absence of structural abnormalities. Initial empiric management, centered on the diagnosis of CA, included fasting and total parenteral nutrition (TPN), followed by a gradual dietary transition from a lipid-free milk formula to a formula enriched in medium-chain triglycerides (MCTs) and reduced in long-chain triglycerides, which was well tolerated. Cytomegalovirus (CMV) infection was identified as the underlying cause and confirmed by PCR on blood, urine, ascitic fluid, and gastric biopsies. The etiological diagnosis allowed for specific antiviral therapy, which, combined with nutritional support, led to complete resolution of the case. We also review published cases of infectious CA in children, analyzing the clinical presentation, diagnostic approaches, and therapeutic strategies. Particular attention is paid to nutritional management. Interventions including the use of TPN, fat-free formulas, or MCT-enriched formulas are also important in infectious etiologies for temporarily controlling the chyle loss mechanism while awaiting complete lymphatic restitution. This is a provisional file, not the final typeset article This review emphasizes the importance of recognizing infectious etiologies in chylous ascites and emphasizes the critical role of personalized nutritional support in optimizing recovery.

Keywords: case report, Chylous ascites (CA), Cytomegalovirus (CMV), lymphatic disease, Parenteral nutrition (PN)

Received: 31 Dec 2025; Accepted: 26 Jan 2026.

Copyright: © 2026 Capriati, Carciofi, Grimaldi, Krzysztofiak, Gatti, Lionetti, Caprarelli, Morelli, Tulli and Diamanti. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Teresa Capriati

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