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Hemolymphangioma of Greater Omentum: A Rare Case Report
Hemolymphangioma is a rare vascular developmental error. It comprises malformed venous and lymphatic component in various proportion. To the best of our knowledge, only a few cases have been reported in the literature so far. Here, we report a case of huge intraperitoneal cystic mass in a 3-year-old...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998721/ https://www.ncbi.nlm.nih.gov/pubmed/27124058 http://dx.doi.org/10.1097/MD.0000000000003508 |
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author | Pandey, Sagar Fan, Miao Chang, Dandan Zhu, Junfeng Zhu, Ying Li, Ziping |
author_facet | Pandey, Sagar Fan, Miao Chang, Dandan Zhu, Junfeng Zhu, Ying Li, Ziping |
author_sort | Pandey, Sagar |
collection | PubMed |
description | Hemolymphangioma is a rare vascular developmental error. It comprises malformed venous and lymphatic component in various proportion. To the best of our knowledge, only a few cases have been reported in the literature so far. Here, we report a case of huge intraperitoneal cystic mass in a 3-year-old boy that was presented to hospital with intractable abdominal pain. On examination, he had fever along with associated symptoms like cough and sputum. Abdomen was distended with no tenderness or rebound tenderness. On computed tomography scan, huge cystic mass was seen and was diagnosed as intraperitoneal benign cystic lesion. Excisional surgery of the lesion was planned. On surgery, lesion was found to be originated from greater omentum and no adhesion was seen in surrounding tissue. Complete excision of the lesion was done. Histopathological specimen after surgery suggested it to be hemolymphangioma. Follow-up for 6 months showed no recurrence. Hemolymphangioma of the greater omentum is benign tumor and accurate diagnosis before surgery is still a challenge. Presentation of disease may vary from simple well-defined cystic lesion to aggressive ill-defined lesion mimicking malignancy. Therefore, further research is needed to help doctor with preoperative radiological diagnosis and avoid unnecessary radical surgery. |
format | Online Article Text |
id | pubmed-4998721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-49987212016-09-06 Hemolymphangioma of Greater Omentum: A Rare Case Report Pandey, Sagar Fan, Miao Chang, Dandan Zhu, Junfeng Zhu, Ying Li, Ziping Medicine (Baltimore) 6800 Hemolymphangioma is a rare vascular developmental error. It comprises malformed venous and lymphatic component in various proportion. To the best of our knowledge, only a few cases have been reported in the literature so far. Here, we report a case of huge intraperitoneal cystic mass in a 3-year-old boy that was presented to hospital with intractable abdominal pain. On examination, he had fever along with associated symptoms like cough and sputum. Abdomen was distended with no tenderness or rebound tenderness. On computed tomography scan, huge cystic mass was seen and was diagnosed as intraperitoneal benign cystic lesion. Excisional surgery of the lesion was planned. On surgery, lesion was found to be originated from greater omentum and no adhesion was seen in surrounding tissue. Complete excision of the lesion was done. Histopathological specimen after surgery suggested it to be hemolymphangioma. Follow-up for 6 months showed no recurrence. Hemolymphangioma of the greater omentum is benign tumor and accurate diagnosis before surgery is still a challenge. Presentation of disease may vary from simple well-defined cystic lesion to aggressive ill-defined lesion mimicking malignancy. Therefore, further research is needed to help doctor with preoperative radiological diagnosis and avoid unnecessary radical surgery. Wolters Kluwer Health 2016-04-29 /pmc/articles/PMC4998721/ /pubmed/27124058 http://dx.doi.org/10.1097/MD.0000000000003508 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | 6800 Pandey, Sagar Fan, Miao Chang, Dandan Zhu, Junfeng Zhu, Ying Li, Ziping Hemolymphangioma of Greater Omentum: A Rare Case Report |
title | Hemolymphangioma of Greater Omentum: A Rare Case Report |
title_full | Hemolymphangioma of Greater Omentum: A Rare Case Report |
title_fullStr | Hemolymphangioma of Greater Omentum: A Rare Case Report |
title_full_unstemmed | Hemolymphangioma of Greater Omentum: A Rare Case Report |
title_short | Hemolymphangioma of Greater Omentum: A Rare Case Report |
title_sort | hemolymphangioma of greater omentum: a rare case report |
topic | 6800 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998721/ https://www.ncbi.nlm.nih.gov/pubmed/27124058 http://dx.doi.org/10.1097/MD.0000000000003508 |
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