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A rare case of retroperitoneal and mesenteric lymphangiomatosis

Lymphagiomatosis are rare benign malformations of the lymphatic system. They are more commonly seen during childhood and are frequently asymptomatic and incidentally found in the adult patient. We report a case of a 31-year-old male who presented initially with melena. Computer tomography scan revea...

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Autores principales: Chan, Wen Yang Shaun, Kwan, Kenneth Eng Ling, Teo, Li Tserng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849486/
https://www.ncbi.nlm.nih.gov/pubmed/31762861
http://dx.doi.org/10.1016/j.radcr.2019.09.039
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author Chan, Wen Yang Shaun
Kwan, Kenneth Eng Ling
Teo, Li Tserng
author_facet Chan, Wen Yang Shaun
Kwan, Kenneth Eng Ling
Teo, Li Tserng
author_sort Chan, Wen Yang Shaun
collection PubMed
description Lymphagiomatosis are rare benign malformations of the lymphatic system. They are more commonly seen during childhood and are frequently asymptomatic and incidentally found in the adult patient. We report a case of a 31-year-old male who presented initially with melena. Computer tomography scan revealed multiple confluent, fluid-density lesions encasing the retroperitoneum and mesentery. A laparotomy and incisional biopsy of the mesenteric lesion was performed. Histologic examination demonstrated fibrofatty tissue with prominent, thick-walled endothelial-lined vessels. The histologic and computer tomography findings were consistent with a diagnosis of retroperitoneal and mesenteric lymphangiomatosis. The patient was subsequently discharged home well.
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spelling pubmed-68494862019-11-22 A rare case of retroperitoneal and mesenteric lymphangiomatosis Chan, Wen Yang Shaun Kwan, Kenneth Eng Ling Teo, Li Tserng Radiol Case Rep Gastrointestinal Lymphagiomatosis are rare benign malformations of the lymphatic system. They are more commonly seen during childhood and are frequently asymptomatic and incidentally found in the adult patient. We report a case of a 31-year-old male who presented initially with melena. Computer tomography scan revealed multiple confluent, fluid-density lesions encasing the retroperitoneum and mesentery. A laparotomy and incisional biopsy of the mesenteric lesion was performed. Histologic examination demonstrated fibrofatty tissue with prominent, thick-walled endothelial-lined vessels. The histologic and computer tomography findings were consistent with a diagnosis of retroperitoneal and mesenteric lymphangiomatosis. The patient was subsequently discharged home well. Elsevier 2019-11-08 /pmc/articles/PMC6849486/ /pubmed/31762861 http://dx.doi.org/10.1016/j.radcr.2019.09.039 Text en © 2019 The Authors. Published by Elsevier Inc. on behalf of University of Washington. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Gastrointestinal
Chan, Wen Yang Shaun
Kwan, Kenneth Eng Ling
Teo, Li Tserng
A rare case of retroperitoneal and mesenteric lymphangiomatosis
title A rare case of retroperitoneal and mesenteric lymphangiomatosis
title_full A rare case of retroperitoneal and mesenteric lymphangiomatosis
title_fullStr A rare case of retroperitoneal and mesenteric lymphangiomatosis
title_full_unstemmed A rare case of retroperitoneal and mesenteric lymphangiomatosis
title_short A rare case of retroperitoneal and mesenteric lymphangiomatosis
title_sort rare case of retroperitoneal and mesenteric lymphangiomatosis
topic Gastrointestinal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849486/
https://www.ncbi.nlm.nih.gov/pubmed/31762861
http://dx.doi.org/10.1016/j.radcr.2019.09.039
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