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Lymphangioma Cavernosum with a Rare Location
Lympangioma cavernosum in the abdominal cavity is a rare benign tumour. In most cases, such tumours are diagnosed in the oral cavity and neck. The aim of this paper is to present our clinical observations and review of existing literature to draw attention to this disease. A 25-year-old woman was ad...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8955802/ https://www.ncbi.nlm.nih.gov/pubmed/35329968 http://dx.doi.org/10.3390/jcm11061643 |
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author | Smaga, Justyna Kornasiewicz, Oskar Ziarkiewicz-Wróblewska, Bogna Podgórska, Joanna Krawczyk, Piotr Grąt, Michał Krawczyk, Marek |
author_facet | Smaga, Justyna Kornasiewicz, Oskar Ziarkiewicz-Wróblewska, Bogna Podgórska, Joanna Krawczyk, Piotr Grąt, Michał Krawczyk, Marek |
author_sort | Smaga, Justyna |
collection | PubMed |
description | Lympangioma cavernosum in the abdominal cavity is a rare benign tumour. In most cases, such tumours are diagnosed in the oral cavity and neck. The aim of this paper is to present our clinical observations and review of existing literature to draw attention to this disease. A 25-year-old woman was admitted to our department for a symptomatic tumour in the lesser curvature of the stomach. The patient was first operated on as a three-year-old child because the tumour extended from the back wall of the stomach to the gastro-colonic ligament. The medical records showed that it was a benign tumour; however, no diagnosis was specified. No symptoms were observed for 22 years. Currently, the patient is admitted for epigastric pain. Abdominal computed tomography revealed an extensive mass located between the left segments of the liver and the lesser curvature of the stomach. The patient was operated on, and the tumour was completely removed. The patient’s postoperative course was uneventful. Histopathological examination of the lymphangioma cavernosum was performed. Two months after the operation, the patient did not report any complaints. |
format | Online Article Text |
id | pubmed-8955802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89558022022-03-26 Lymphangioma Cavernosum with a Rare Location Smaga, Justyna Kornasiewicz, Oskar Ziarkiewicz-Wróblewska, Bogna Podgórska, Joanna Krawczyk, Piotr Grąt, Michał Krawczyk, Marek J Clin Med Case Report Lympangioma cavernosum in the abdominal cavity is a rare benign tumour. In most cases, such tumours are diagnosed in the oral cavity and neck. The aim of this paper is to present our clinical observations and review of existing literature to draw attention to this disease. A 25-year-old woman was admitted to our department for a symptomatic tumour in the lesser curvature of the stomach. The patient was first operated on as a three-year-old child because the tumour extended from the back wall of the stomach to the gastro-colonic ligament. The medical records showed that it was a benign tumour; however, no diagnosis was specified. No symptoms were observed for 22 years. Currently, the patient is admitted for epigastric pain. Abdominal computed tomography revealed an extensive mass located between the left segments of the liver and the lesser curvature of the stomach. The patient was operated on, and the tumour was completely removed. The patient’s postoperative course was uneventful. Histopathological examination of the lymphangioma cavernosum was performed. Two months after the operation, the patient did not report any complaints. MDPI 2022-03-16 /pmc/articles/PMC8955802/ /pubmed/35329968 http://dx.doi.org/10.3390/jcm11061643 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Smaga, Justyna Kornasiewicz, Oskar Ziarkiewicz-Wróblewska, Bogna Podgórska, Joanna Krawczyk, Piotr Grąt, Michał Krawczyk, Marek Lymphangioma Cavernosum with a Rare Location |
title | Lymphangioma Cavernosum with a Rare Location |
title_full | Lymphangioma Cavernosum with a Rare Location |
title_fullStr | Lymphangioma Cavernosum with a Rare Location |
title_full_unstemmed | Lymphangioma Cavernosum with a Rare Location |
title_short | Lymphangioma Cavernosum with a Rare Location |
title_sort | lymphangioma cavernosum with a rare location |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8955802/ https://www.ncbi.nlm.nih.gov/pubmed/35329968 http://dx.doi.org/10.3390/jcm11061643 |
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