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Sclerosing Angiomatoid Nodular Transformation of the Spleen: A Diagnostic Conundrum

A splenic lesion often represents a diagnostic challenge due to relative scarcity and the broad differential diagnosis. Sclerosing Angiomatoid Nodular Transformation (SANT) of the spleen is usually encountered only incidentally. Although benign, patients with SANT often receive splenectomy, due to i...

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Autores principales: Van den Eede, Sander, Van de Voorde, Nick, Vanhoenacker, Filip, Op de Beeck, Bart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ubiquity Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8992766/
https://www.ncbi.nlm.nih.gov/pubmed/35480339
http://dx.doi.org/10.5334/jbsr.2689
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author Van den Eede, Sander
Van de Voorde, Nick
Vanhoenacker, Filip
Op de Beeck, Bart
author_facet Van den Eede, Sander
Van de Voorde, Nick
Vanhoenacker, Filip
Op de Beeck, Bart
author_sort Van den Eede, Sander
collection PubMed
description A splenic lesion often represents a diagnostic challenge due to relative scarcity and the broad differential diagnosis. Sclerosing Angiomatoid Nodular Transformation (SANT) of the spleen is usually encountered only incidentally. Although benign, patients with SANT often receive splenectomy, due to its rarity, diagnostic uncertainty and sometimes intimidating imaging morphology and size. Imaging features on computed tomography, magnetic resonance and positron emission tomography have a high diagnostic value for SANT and help differentiate this entity from other splenic lesions. When the imaging parameters are matched with core needle biopsy tissue analysis, further watchful waiting can be recommended in order to avoid splenectomy.
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spelling pubmed-89927662022-04-26 Sclerosing Angiomatoid Nodular Transformation of the Spleen: A Diagnostic Conundrum Van den Eede, Sander Van de Voorde, Nick Vanhoenacker, Filip Op de Beeck, Bart J Belg Soc Radiol Review Article A splenic lesion often represents a diagnostic challenge due to relative scarcity and the broad differential diagnosis. Sclerosing Angiomatoid Nodular Transformation (SANT) of the spleen is usually encountered only incidentally. Although benign, patients with SANT often receive splenectomy, due to its rarity, diagnostic uncertainty and sometimes intimidating imaging morphology and size. Imaging features on computed tomography, magnetic resonance and positron emission tomography have a high diagnostic value for SANT and help differentiate this entity from other splenic lesions. When the imaging parameters are matched with core needle biopsy tissue analysis, further watchful waiting can be recommended in order to avoid splenectomy. Ubiquity Press 2022-04-05 /pmc/articles/PMC8992766/ /pubmed/35480339 http://dx.doi.org/10.5334/jbsr.2689 Text en Copyright: © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (CC-BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. See http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review Article
Van den Eede, Sander
Van de Voorde, Nick
Vanhoenacker, Filip
Op de Beeck, Bart
Sclerosing Angiomatoid Nodular Transformation of the Spleen: A Diagnostic Conundrum
title Sclerosing Angiomatoid Nodular Transformation of the Spleen: A Diagnostic Conundrum
title_full Sclerosing Angiomatoid Nodular Transformation of the Spleen: A Diagnostic Conundrum
title_fullStr Sclerosing Angiomatoid Nodular Transformation of the Spleen: A Diagnostic Conundrum
title_full_unstemmed Sclerosing Angiomatoid Nodular Transformation of the Spleen: A Diagnostic Conundrum
title_short Sclerosing Angiomatoid Nodular Transformation of the Spleen: A Diagnostic Conundrum
title_sort sclerosing angiomatoid nodular transformation of the spleen: a diagnostic conundrum
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8992766/
https://www.ncbi.nlm.nih.gov/pubmed/35480339
http://dx.doi.org/10.5334/jbsr.2689
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