Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Smaga, Justyna, Kornasiewicz, Oskar, Ziarkiewicz-Wróblewska, Bogna, Podgórska, Joanna, Krawczyk, Piotr, Grąt, Michał, Krawczyk, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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
_version_ 1784676426133274624
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
work_keys_str_mv AT smagajustyna lymphangiomacavernosumwithararelocation
AT kornasiewiczoskar lymphangiomacavernosumwithararelocation
AT ziarkiewiczwroblewskabogna lymphangiomacavernosumwithararelocation
AT podgorskajoanna lymphangiomacavernosumwithararelocation
AT krawczykpiotr lymphangiomacavernosumwithararelocation
AT gratmichał lymphangiomacavernosumwithararelocation
AT krawczykmarek lymphangiomacavernosumwithararelocation