gms | German Medical Science

133. Kongress der Deutschen Gesellschaft für Chirurgie

Deutsche Gesellschaft für Chirurgie

26.04. - 29.04.2016, Berlin

Benigne mesenteric lymphangioma in children – three cases varying exceedingly in clinical presentation

Meeting Abstract

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  • Christiane Barthel - Klinikum Nürnberg Süd, Kinderchirurgie, Nürnberg, Deutschland

Deutsche Gesellschaft für Chirurgie. 133. Kongress der Deutschen Gesellschaft für Chirurgie. Berlin, 26.-29.04.2016. Düsseldorf: German Medical Science GMS Publishing House; 2016. Doc16dgch272

doi: 10.3205/16dgch272, urn:nbn:de:0183-16dgch2728

Published: April 21, 2016

© 2016 Barthel.
This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License. See license information at http://creativecommons.org/licenses/by/4.0/.


Outline

Text

Background: Mesenteric cysts are rare findings, especially in children under the age of 10. As one type of these cysts small-bowel mesentery lymphangioma occur in only 1 % of cases with lymphangioma. The majority of these tumors however, are localized in head or neck areas. We treated three patients matching both criteria: children even under the age of 5 with the histological diagnosis of mesenteric lymphangioma.

Materials and methods: Varying considerably in clinical presentation, sonographic findings and laboratory work we present three girls under the age of 5 with mesenteric lymphangioma from May to September 2015. Every case is documented from time of first encounter, clinical work-up, intra-operative findings to post-treatment care.

Results: The first patient presented with acute abdominal tenderness, periumbilical tenderness on palpation, elevated inflammatory values and unremarkable abdominal ultrasound. The second patient had a history of chronic abdominal pain and constipation for half a year, one episode of urinary retention presenting with strong abdominal pain upon admission. Her laboratory work-up was unremarkable, however sonography showed three large cystic formations in the lower abdomen. The third girl presented with continuous vomiting, leukocytosis and the sonographic finding of a cystic structure in the lower abdomen. In each case the resected tissue was confirmed by histology to be mesenteric lymphangioma.

In two cases we partially resected small bowel, resulting in en bloc removal of the lymphangioma. In one case the cysts were too large and wide-spread to be removed without losing significant bowel tissue. In that case we partially resected the three main cystic formations.

Conclusion: Mesenteric lymphangioma can mimic several abdominal conditions. It should therefore be considered as a rare but significant differential diagnosis to acute appendicitis, ovarian torsion, volvulus and incarcerated meckel´s diverticulum. Due to the difficulty in diagnosis especially in this age group, they pose a significant challenge for treating physicians.