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Splenic lymphangioma
INTRODUCTION: Abdominal localization of cyst lymphangioma is rare. The splenic involvement is exceptional. CASE PRESENTATION: A 63-year-old woman, who was followed for martial anemia evolving associated with abdominal pain in the past 12 months. On clinical examination, she had pallor conjunctival m...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717100/ https://www.ncbi.nlm.nih.gov/pubmed/31430605 http://dx.doi.org/10.1016/j.ijscr.2019.07.078 |
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author | Ousmane, Thiam Mamadou, Faye Papa Sitor, Sarr Ibrahima Abdou, Niasse Madieng, Dieng |
author_facet | Ousmane, Thiam Mamadou, Faye Papa Sitor, Sarr Ibrahima Abdou, Niasse Madieng, Dieng |
author_sort | Ousmane, Thiam |
collection | PubMed |
description | INTRODUCTION: Abdominal localization of cyst lymphangioma is rare. The splenic involvement is exceptional. CASE PRESENTATION: A 63-year-old woman, who was followed for martial anemia evolving associated with abdominal pain in the past 12 months. On clinical examination, she had pallor conjunctival mucosa, with a normal abdominal and lymph node examination. The abdominal ultrasound showed multiple splenic cysts. The abdominal CT scan showed a normal-sized spleen with multiples hypodense cystic lesions. At the laparotomy exploration a multinodular spleen was found which measured 18 cm*15 cm*6 cm. The histological exam results showed concluded to a splenic cavernous lymphangioma without malignity signs. The follow-up after 12 months was normal. CONCLUSION: splenic lymphangioma is rare and benign tumor. Total splenectomy under laparotomy or laparoscopy is the appropriate treatment. |
format | Online Article Text |
id | pubmed-6717100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-67171002019-09-04 Splenic lymphangioma Ousmane, Thiam Mamadou, Faye Papa Sitor, Sarr Ibrahima Abdou, Niasse Madieng, Dieng Int J Surg Case Rep Article INTRODUCTION: Abdominal localization of cyst lymphangioma is rare. The splenic involvement is exceptional. CASE PRESENTATION: A 63-year-old woman, who was followed for martial anemia evolving associated with abdominal pain in the past 12 months. On clinical examination, she had pallor conjunctival mucosa, with a normal abdominal and lymph node examination. The abdominal ultrasound showed multiple splenic cysts. The abdominal CT scan showed a normal-sized spleen with multiples hypodense cystic lesions. At the laparotomy exploration a multinodular spleen was found which measured 18 cm*15 cm*6 cm. The histological exam results showed concluded to a splenic cavernous lymphangioma without malignity signs. The follow-up after 12 months was normal. CONCLUSION: splenic lymphangioma is rare and benign tumor. Total splenectomy under laparotomy or laparoscopy is the appropriate treatment. Elsevier 2019-08-08 /pmc/articles/PMC6717100/ /pubmed/31430605 http://dx.doi.org/10.1016/j.ijscr.2019.07.078 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ousmane, Thiam Mamadou, Faye Papa Sitor, Sarr Ibrahima Abdou, Niasse Madieng, Dieng Splenic lymphangioma |
title | Splenic lymphangioma |
title_full | Splenic lymphangioma |
title_fullStr | Splenic lymphangioma |
title_full_unstemmed | Splenic lymphangioma |
title_short | Splenic lymphangioma |
title_sort | splenic lymphangioma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6717100/ https://www.ncbi.nlm.nih.gov/pubmed/31430605 http://dx.doi.org/10.1016/j.ijscr.2019.07.078 |
work_keys_str_mv | AT ousmanethiam spleniclymphangioma AT mamadoufayepapa spleniclymphangioma AT sitorsarribrahima spleniclymphangioma AT abdouniasse spleniclymphangioma AT madiengdieng spleniclymphangioma |