ArticleJournal of surgical case reports2020
Giant lymphatic malformation causing abdominal compartment syndrome in a neonate: a rare surgical emergency.
Article in Journal of surgical case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 6 citations in OpenAlex.
- Neonatal liver tumors requiring early postnatal hepatectomy: A retrospective review of seven cases.Surgery today · 2026Article
- Laparoscopic-assisted sclerotherapy in pediatric retroperitoneal lymphatic malformations.Frontiers in pediatrics · 2024Article
- Laparoscopic surgery of intra-abdominal lymphatic malformation in children.Experimental and therapeutic medicine · 2022Article
- Tumor or Inflammatory Myofibroblastic Reaction in an Adolescent With an Abdominal Lymphatic Malformation?Cureus · 2022Article
- Mesenteric Cyst with GI Symptoms: A Fluid Approach to Treatment-Case Report and Literature Review.Digestive diseases and sciences · 2022Review
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Authors and funding
6 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
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.
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