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Giant lymphatic malformation causing abdominal compartment syndrome in a neonate: a rare surgical emergency
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 h...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7449550/ https://www.ncbi.nlm.nih.gov/pubmed/32874540 http://dx.doi.org/10.1093/jscr/rjaa252 |
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author | Gasparella, Paolo Singer, Georg Castellani, Christoph Sorantin, Erich Haxhija, Emir Q Till, Holger |
author_facet | Gasparella, Paolo Singer, Georg Castellani, Christoph Sorantin, Erich Haxhija, Emir Q Till, Holger |
author_sort | Gasparella, Paolo |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7449550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-74495502020-08-31 Giant lymphatic malformation causing abdominal compartment syndrome in a neonate: a rare surgical emergency Gasparella, Paolo Singer, Georg Castellani, Christoph Sorantin, Erich Haxhija, Emir Q Till, Holger J Surg Case Rep Case Report 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. Oxford University Press 2020-08-26 /pmc/articles/PMC7449550/ /pubmed/32874540 http://dx.doi.org/10.1093/jscr/rjaa252 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2020. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Report Gasparella, Paolo Singer, Georg Castellani, Christoph Sorantin, Erich Haxhija, Emir Q Till, Holger Giant lymphatic malformation causing abdominal compartment syndrome in a neonate: a rare surgical emergency |
title | Giant lymphatic malformation causing abdominal compartment syndrome in a neonate: a rare surgical emergency |
title_full | Giant lymphatic malformation causing abdominal compartment syndrome in a neonate: a rare surgical emergency |
title_fullStr | Giant lymphatic malformation causing abdominal compartment syndrome in a neonate: a rare surgical emergency |
title_full_unstemmed | Giant lymphatic malformation causing abdominal compartment syndrome in a neonate: a rare surgical emergency |
title_short | Giant lymphatic malformation causing abdominal compartment syndrome in a neonate: a rare surgical emergency |
title_sort | giant lymphatic malformation causing abdominal compartment syndrome in a neonate: a rare surgical emergency |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7449550/ https://www.ncbi.nlm.nih.gov/pubmed/32874540 http://dx.doi.org/10.1093/jscr/rjaa252 |
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