Mesenteric polycystic lymphangiomatosis in a pediatric patient. Case report

Authors

DOI:

https://doi.org/10.56294/piii2024343

Keywords:

Mesenteric polycystic lymphangiomas, abdominal cystic tumor, mesentery

Abstract

Introduction: Mesenteric polycystic lymphangiomas are rare cystic tumors, with a 5% incidence compared to their incidence in the neck and axillae (95%), seen more frequently in pediatric patients, rare in patients over 20 years of age.
Clinical case: A 3-year-old male patient presents with a clinical picture of one day of evolution, reporting abdominal pain of moderate intensity, temperature rises and vomiting. Physical findings show abdominal distension, with ultrasound showing a polycystic lesion, and contrast-enhanced tomography corroborating a lobulated multi-separated cystic formation. Exploratory laparotomy revealed a polycystic tumor at the level of the ileum mesentery. The anatomopathological study describes a polycystic mesenteric lesion. Exeresis is performed and the postoperative evolution is satisfactory.
Conclusions: Polycystic mesenteric lymphangiomatosis is a rare tumor that mainly affects the mesentery of the small intestine and/or colon. In pediatric age, this condition should be considered as a differential diagnosis of acute abdomen. Conventional or laparoscopic surgery is the cornerstone of treatment

References

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Published

2024-06-12

How to Cite

1.
Callizaya Macedo G, Auza-Santivañez JC, Cussi Quitihuari ER, Vallejos Rejas DRE, Antezana-Muñoz JB, Zurita Villazón M. Mesenteric polycystic lymphangiomatosis in a pediatric patient. Case report. SCT Proceedings in Interdisciplinary Insights and Innovations [Internet]. 2024 Jun. 12 [cited 2024 Oct. 7];2:343. Available from: https://proceedings.ageditor.ar/index.php/piii/article/view/308