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Cause exceptionnelle d'hémoperitoine spontané chez l'adulte: hémolymphangiome kystique rompu
Hemolymphangioma is a benign tumor resulting from the abnormal development of the lymphatic vessels associated with vascular malformations. 50% to 60% of these tumours are present at birth. Cervical forms are most frequent. Abdominales locations are very rare. We report, through a literature review,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398216/ https://www.ncbi.nlm.nih.gov/pubmed/28450987 http://dx.doi.org/10.11604/pamj.2017.26.8.6533 |
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author | Traoré, Boubacar Zan Serrar, Kamal Saoud, Omar El Abidine, Khedid Yahia Zain Chkoff, Rachid Mohammed M'bida, Rachida |
author_facet | Traoré, Boubacar Zan Serrar, Kamal Saoud, Omar El Abidine, Khedid Yahia Zain Chkoff, Rachid Mohammed M'bida, Rachida |
author_sort | Traoré, Boubacar Zan |
collection | PubMed |
description | Hemolymphangioma is a benign tumor resulting from the abnormal development of the lymphatic vessels associated with vascular malformations. 50% to 60% of these tumours are present at birth. Cervical forms are most frequent. Abdominales locations are very rare. We report, through a literature review, two cases of patients with cystic hemolymphangioma of the spleen revealed by spontaneous haemoperitoneum admitted to the Emergency Department of Visceral Surgery. The first case is a 50-year old patient and the second is 20-year old man admitted to the emergency department with diffuse abdominal pain associated with dullness to percussion on the dependent side and abdominal distension associated with haemorrhagic shock, pallor, unobtainable pulse, stabilized after a short resuscitation time respectively. All patients underwent complete tumor resection. The diagnosis of cystic hemolymphangioma of the spleen was based on anatomopathological examination of the surgical specimens. Hemolymphangioma is a rare tumor with a favorable prognosis. Some cases of spontaneous regression have been reported, but evolution is usually characterized by slow tumor growth. Malignant transformation never occurs. Treatment is surgical. Prognosis is subjected to complications, quality of the surgical excision and recurrences which are frequent especially after incomplete excision. |
format | Online Article Text |
id | pubmed-5398216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-53982162017-04-27 Cause exceptionnelle d'hémoperitoine spontané chez l'adulte: hémolymphangiome kystique rompu Traoré, Boubacar Zan Serrar, Kamal Saoud, Omar El Abidine, Khedid Yahia Zain Chkoff, Rachid Mohammed M'bida, Rachida Pan Afr Med J Case Report Hemolymphangioma is a benign tumor resulting from the abnormal development of the lymphatic vessels associated with vascular malformations. 50% to 60% of these tumours are present at birth. Cervical forms are most frequent. Abdominales locations are very rare. We report, through a literature review, two cases of patients with cystic hemolymphangioma of the spleen revealed by spontaneous haemoperitoneum admitted to the Emergency Department of Visceral Surgery. The first case is a 50-year old patient and the second is 20-year old man admitted to the emergency department with diffuse abdominal pain associated with dullness to percussion on the dependent side and abdominal distension associated with haemorrhagic shock, pallor, unobtainable pulse, stabilized after a short resuscitation time respectively. All patients underwent complete tumor resection. The diagnosis of cystic hemolymphangioma of the spleen was based on anatomopathological examination of the surgical specimens. Hemolymphangioma is a rare tumor with a favorable prognosis. Some cases of spontaneous regression have been reported, but evolution is usually characterized by slow tumor growth. Malignant transformation never occurs. Treatment is surgical. Prognosis is subjected to complications, quality of the surgical excision and recurrences which are frequent especially after incomplete excision. The African Field Epidemiology Network 2017-01-04 /pmc/articles/PMC5398216/ /pubmed/28450987 http://dx.doi.org/10.11604/pamj.2017.26.8.6533 Text en © Boubacar Zan Traoré et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of 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 Traoré, Boubacar Zan Serrar, Kamal Saoud, Omar El Abidine, Khedid Yahia Zain Chkoff, Rachid Mohammed M'bida, Rachida Cause exceptionnelle d'hémoperitoine spontané chez l'adulte: hémolymphangiome kystique rompu |
title | Cause exceptionnelle d'hémoperitoine spontané chez l'adulte: hémolymphangiome kystique rompu |
title_full | Cause exceptionnelle d'hémoperitoine spontané chez l'adulte: hémolymphangiome kystique rompu |
title_fullStr | Cause exceptionnelle d'hémoperitoine spontané chez l'adulte: hémolymphangiome kystique rompu |
title_full_unstemmed | Cause exceptionnelle d'hémoperitoine spontané chez l'adulte: hémolymphangiome kystique rompu |
title_short | Cause exceptionnelle d'hémoperitoine spontané chez l'adulte: hémolymphangiome kystique rompu |
title_sort | cause exceptionnelle d'hémoperitoine spontané chez l'adulte: hémolymphangiome kystique rompu |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398216/ https://www.ncbi.nlm.nih.gov/pubmed/28450987 http://dx.doi.org/10.11604/pamj.2017.26.8.6533 |
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