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Laparoscopic splenectomy for sclerosing angiomatoid nodular transformation of the spleen

Sclerosing angiomatoid nodular transformation (SANT) is a rare, benign, proliferative vascular lesion that arises from the splenic red pulp. Most patients with SANT have no clinical symptoms and are discovered incidentally on imaging. There are no definitive radiological signs and a distinction from...

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Autores principales: Bushati, Matilda, Sommariva, Antonio, Montesco, Maria Cristina, Rossi, Carlo Riccardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607801/
https://www.ncbi.nlm.nih.gov/pubmed/28695885
http://dx.doi.org/10.4103/jmas.JMAS_95_16
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author Bushati, Matilda
Sommariva, Antonio
Montesco, Maria Cristina
Rossi, Carlo Riccardo
author_facet Bushati, Matilda
Sommariva, Antonio
Montesco, Maria Cristina
Rossi, Carlo Riccardo
author_sort Bushati, Matilda
collection PubMed
description Sclerosing angiomatoid nodular transformation (SANT) is a rare, benign, proliferative vascular lesion that arises from the splenic red pulp. Most patients with SANT have no clinical symptoms and are discovered incidentally on imaging. There are no definitive radiological signs and a distinction from other splenic diseases, and malignant processes remain difficult. Confirmation of the diagnosis of SANT requires a histological and immunohistochemical evaluation of the resected spleen. Here, we report an unusual case of SANT of the spleen successfully treated with an elective laparoscopic splenectomy (LS). LS is a safe and effective method for diagnosis of SANT.
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spelling pubmed-56078012017-10-01 Laparoscopic splenectomy for sclerosing angiomatoid nodular transformation of the spleen Bushati, Matilda Sommariva, Antonio Montesco, Maria Cristina Rossi, Carlo Riccardo J Minim Access Surg Unusual Case Sclerosing angiomatoid nodular transformation (SANT) is a rare, benign, proliferative vascular lesion that arises from the splenic red pulp. Most patients with SANT have no clinical symptoms and are discovered incidentally on imaging. There are no definitive radiological signs and a distinction from other splenic diseases, and malignant processes remain difficult. Confirmation of the diagnosis of SANT requires a histological and immunohistochemical evaluation of the resected spleen. Here, we report an unusual case of SANT of the spleen successfully treated with an elective laparoscopic splenectomy (LS). LS is a safe and effective method for diagnosis of SANT. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5607801/ /pubmed/28695885 http://dx.doi.org/10.4103/jmas.JMAS_95_16 Text en Copyright: © 2017 Journal of Minimal Access Surgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Unusual Case
Bushati, Matilda
Sommariva, Antonio
Montesco, Maria Cristina
Rossi, Carlo Riccardo
Laparoscopic splenectomy for sclerosing angiomatoid nodular transformation of the spleen
title Laparoscopic splenectomy for sclerosing angiomatoid nodular transformation of the spleen
title_full Laparoscopic splenectomy for sclerosing angiomatoid nodular transformation of the spleen
title_fullStr Laparoscopic splenectomy for sclerosing angiomatoid nodular transformation of the spleen
title_full_unstemmed Laparoscopic splenectomy for sclerosing angiomatoid nodular transformation of the spleen
title_short Laparoscopic splenectomy for sclerosing angiomatoid nodular transformation of the spleen
title_sort laparoscopic splenectomy for sclerosing angiomatoid nodular transformation of the spleen
topic Unusual Case
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607801/
https://www.ncbi.nlm.nih.gov/pubmed/28695885
http://dx.doi.org/10.4103/jmas.JMAS_95_16
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