Giant lymphatic malformation causing abdominal compartment syndrome in a neonate: a rare surgical emergency.
Paolo GasparellaGeorg SingerChristoph CastellaniErich SorantinEmir Q HaxhijaHolger TillPublished in: Journal of surgical case reports (2020)
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.
Keyphrases
- lymph node
- emergency department
- randomized controlled trial
- magnetic resonance imaging
- public health
- liver failure
- intensive care unit
- high resolution
- magnetic resonance
- cognitive impairment
- low birth weight
- body mass index
- computed tomography
- coronary artery bypass
- photodynamic therapy
- mass spectrometry
- weight loss
- hepatitis b virus
- study protocol
- prognostic factors
- rare case
- birth weight
- double blind