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Giant mesenteric cystic lymphangioma of mesocolic origin in an asymptomatic adult patient

A 34-year-old patient was scheduled for valve replacement to treat a symptomatic mitral regurgitation. The preoperative work-up incidentally discovered an intra-abdominal cystic tumour extending from the epigastrium to the pelvic region on a computed tomography scan. The patient had no abdominal sym...

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Autores principales: Kambakamba, P, Lesurtel, M, Breitenstein, S, Emmert, MY, Wilhelm, MJ, Clavien, PA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JSCR Publishing Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3862254/
https://www.ncbi.nlm.nih.gov/pubmed/24960673
http://dx.doi.org/10.1093/jscr/2012.6.4
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author Kambakamba, P
Lesurtel, M
Breitenstein, S
Emmert, MY
Wilhelm, MJ
Clavien, PA
author_facet Kambakamba, P
Lesurtel, M
Breitenstein, S
Emmert, MY
Wilhelm, MJ
Clavien, PA
author_sort Kambakamba, P
collection PubMed
description A 34-year-old patient was scheduled for valve replacement to treat a symptomatic mitral regurgitation. The preoperative work-up incidentally discovered an intra-abdominal cystic tumour extending from the epigastrium to the pelvic region on a computed tomography scan. The patient had no abdominal symptoms by the giant cyst from unkown origin. An open “en bloc” resection disclosed a large cyst in the mesocolon. Pathological examination, including immunohistochemistry, enabled the diagnosis of a mesenteric cystic lymphangioma. Long-term follow-up of 12 months shows no recurrence. Mesenteric cystic lymphangioma, which is extremely rare in adults, is a challenge to diagnose and needs complete resection to ensure dignity and to avoid recurrence.
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spelling pubmed-38622542013-12-18 Giant mesenteric cystic lymphangioma of mesocolic origin in an asymptomatic adult patient Kambakamba, P Lesurtel, M Breitenstein, S Emmert, MY Wilhelm, MJ Clavien, PA J Surg Case Rep Colorectal Surgery A 34-year-old patient was scheduled for valve replacement to treat a symptomatic mitral regurgitation. The preoperative work-up incidentally discovered an intra-abdominal cystic tumour extending from the epigastrium to the pelvic region on a computed tomography scan. The patient had no abdominal symptoms by the giant cyst from unkown origin. An open “en bloc” resection disclosed a large cyst in the mesocolon. Pathological examination, including immunohistochemistry, enabled the diagnosis of a mesenteric cystic lymphangioma. Long-term follow-up of 12 months shows no recurrence. Mesenteric cystic lymphangioma, which is extremely rare in adults, is a challenge to diagnose and needs complete resection to ensure dignity and to avoid recurrence. JSCR Publishing Ltd 2012-06-01 /pmc/articles/PMC3862254/ /pubmed/24960673 http://dx.doi.org/10.1093/jscr/2012.6.4 Text en © JSCR
spellingShingle Colorectal Surgery
Kambakamba, P
Lesurtel, M
Breitenstein, S
Emmert, MY
Wilhelm, MJ
Clavien, PA
Giant mesenteric cystic lymphangioma of mesocolic origin in an asymptomatic adult patient
title Giant mesenteric cystic lymphangioma of mesocolic origin in an asymptomatic adult patient
title_full Giant mesenteric cystic lymphangioma of mesocolic origin in an asymptomatic adult patient
title_fullStr Giant mesenteric cystic lymphangioma of mesocolic origin in an asymptomatic adult patient
title_full_unstemmed Giant mesenteric cystic lymphangioma of mesocolic origin in an asymptomatic adult patient
title_short Giant mesenteric cystic lymphangioma of mesocolic origin in an asymptomatic adult patient
title_sort giant mesenteric cystic lymphangioma of mesocolic origin in an asymptomatic adult patient
topic Colorectal Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3862254/
https://www.ncbi.nlm.nih.gov/pubmed/24960673
http://dx.doi.org/10.1093/jscr/2012.6.4
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