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Omental Lymphangioma in Adults—Rare Presentation Report of a Case

Lymphangioma is an uncommon benign lesion that usually occurs during childhood. Its occurrence in adults is rare. Its presentation in the abdomen is even rare. This case report describes a case of omental lymphangioma presented as retroperitoneal lump. Subsequent imaging, operative, and histological...

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Autores principales: Rao, T. Narayana, Parvathi, T., Suvarchala, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502815/
https://www.ncbi.nlm.nih.gov/pubmed/23198248
http://dx.doi.org/10.1155/2012/629482
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author Rao, T. Narayana
Parvathi, T.
Suvarchala, A.
author_facet Rao, T. Narayana
Parvathi, T.
Suvarchala, A.
author_sort Rao, T. Narayana
collection PubMed
description Lymphangioma is an uncommon benign lesion that usually occurs during childhood. Its occurrence in adults is rare. Its presentation in the abdomen is even rare. This case report describes a case of omental lymphangioma presented as retroperitoneal lump. Subsequent imaging, operative, and histological findings revealed omental lymphangioma. Laparotomy done under general anesthesia, a 10 × 12 cm cystic swelling arising from omentum, identified complete excision of the cyst done and send the specimen for histopathological examination. Biopsy report came as omental lymphangioma. Complete surgical excision is the treatment of choice. Prognosis is excellent and recurrence rate is very low if resection is complete. During two years of followup no recurrence was detected. Omental lymphangioma is very rare presentation among abdominal lymphangiomas specifically in adults. Complete excision is the treatment of choice. Long-term followup is required to detect recurrence.
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spelling pubmed-35028152012-11-29 Omental Lymphangioma in Adults—Rare Presentation Report of a Case Rao, T. Narayana Parvathi, T. Suvarchala, A. Case Rep Surg Case Report Lymphangioma is an uncommon benign lesion that usually occurs during childhood. Its occurrence in adults is rare. Its presentation in the abdomen is even rare. This case report describes a case of omental lymphangioma presented as retroperitoneal lump. Subsequent imaging, operative, and histological findings revealed omental lymphangioma. Laparotomy done under general anesthesia, a 10 × 12 cm cystic swelling arising from omentum, identified complete excision of the cyst done and send the specimen for histopathological examination. Biopsy report came as omental lymphangioma. Complete surgical excision is the treatment of choice. Prognosis is excellent and recurrence rate is very low if resection is complete. During two years of followup no recurrence was detected. Omental lymphangioma is very rare presentation among abdominal lymphangiomas specifically in adults. Complete excision is the treatment of choice. Long-term followup is required to detect recurrence. Hindawi Publishing Corporation 2012 2012-11-06 /pmc/articles/PMC3502815/ /pubmed/23198248 http://dx.doi.org/10.1155/2012/629482 Text en Copyright © 2012 T. Narayana Rao et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Rao, T. Narayana
Parvathi, T.
Suvarchala, A.
Omental Lymphangioma in Adults—Rare Presentation Report of a Case
title Omental Lymphangioma in Adults—Rare Presentation Report of a Case
title_full Omental Lymphangioma in Adults—Rare Presentation Report of a Case
title_fullStr Omental Lymphangioma in Adults—Rare Presentation Report of a Case
title_full_unstemmed Omental Lymphangioma in Adults—Rare Presentation Report of a Case
title_short Omental Lymphangioma in Adults—Rare Presentation Report of a Case
title_sort omental lymphangioma in adults—rare presentation report of a case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502815/
https://www.ncbi.nlm.nih.gov/pubmed/23198248
http://dx.doi.org/10.1155/2012/629482
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