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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...

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Autores principales: Ousmane, Thiam, Mamadou, Faye Papa, Sitor, Sarr Ibrahima, Abdou, Niasse, Madieng, Dieng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
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.
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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
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AT abdouniasse spleniclymphangioma
AT madiengdieng spleniclymphangioma