Giant lymphatic malformation causing abdominal compartment syndrome in a neonate: a rare surgical emergency

Author:

Gasparella Paolo1ORCID,Singer Georg1,Castellani Christoph1,Sorantin Erich2,Haxhija Emir Q1,Till Holger1

Affiliation:

1. Department of Paediatric and Adolescent Surgery, Medical University of Graz, Graz, Austria

2. Division of Paediatric Radiology, Department of Radiology, Medical University of Graz, Graz, Austria

Abstract

Abstract Abdominal lymphatic malformations in neonates require sophisticated management. In symptomatic cases, acute complications may necessitate immediate surgery. We present the case of a giant abdominal lymphatic malformation diagnosed in the 18th gestational week. Sonographic concerns about intestinal hypoperfusion in the 33rd week of gestation indicated caesarean section. Postnatal imaging confirmed a macrocystic lymphatic malformation occupying almost the complete abdominal cavity; the intestinal perfusion was normal. Clinical deterioration on Day 13 of life required laparotomy. Intraoperatively, the lymphatic mass was located in the ileocecal mesentery. Two major cysts showed recent hemorrhage explaining the onset of abdominal compartment syndrome. The malformation was completely removed. An ileocecal resection with an ileocolic anastomosis was performed. The postoperative course was uneventful. In neonates with abdominal lymphatic malformations, an onset of abdominal compartment syndrome requires surgical exploration. If feasible, the complete removal of the lesion represents a curative option.

Publisher

Oxford University Press (OUP)

Subject

Surgery

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