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Mazabraud's syndrome: case report and literature review

Mazabraud's syndrome is a rare disorder characterized by the association of single or multiple intramuscular myxomas with fibrous dysplasia. Here, we present the first case of Mazabraud's syndrome visualized on 18F-FDG PET/CT with histopathological confirmation of the myxoma. Our case demo...

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Autores principales: Munksgaard, Peter Svenssen, Salkus, Giedrius, Iyer, Victor V, Fisker, Rune Vincents
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3805425/
https://www.ncbi.nlm.nih.gov/pubmed/24198959
http://dx.doi.org/10.1177/2047981613492532
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author Munksgaard, Peter Svenssen
Salkus, Giedrius
Iyer, Victor V
Fisker, Rune Vincents
author_facet Munksgaard, Peter Svenssen
Salkus, Giedrius
Iyer, Victor V
Fisker, Rune Vincents
author_sort Munksgaard, Peter Svenssen
collection PubMed
description Mazabraud's syndrome is a rare disorder characterized by the association of single or multiple intramuscular myxomas with fibrous dysplasia. Here, we present the first case of Mazabraud's syndrome visualized on 18F-FDG PET/CT with histopathological confirmation of the myxoma. Our case demonstrates a slightly increased FDG uptake (SUVmax 2.1) within the myxomas and a moderately to highly increased tracer uptake (SUVmax 7.0) within the fibrous dysplastic lesions. The typical histological appearance of the intramuscular myxoma confirmed the radiological diagnosis. Further, we discuss the imaging findings and the histopathological features of this rare case with a review of the related literature.
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spelling pubmed-38054252013-11-06 Mazabraud's syndrome: case report and literature review Munksgaard, Peter Svenssen Salkus, Giedrius Iyer, Victor V Fisker, Rune Vincents Acta Radiol Short Rep Case Report Mazabraud's syndrome is a rare disorder characterized by the association of single or multiple intramuscular myxomas with fibrous dysplasia. Here, we present the first case of Mazabraud's syndrome visualized on 18F-FDG PET/CT with histopathological confirmation of the myxoma. Our case demonstrates a slightly increased FDG uptake (SUVmax 2.1) within the myxomas and a moderately to highly increased tracer uptake (SUVmax 7.0) within the fibrous dysplastic lesions. The typical histological appearance of the intramuscular myxoma confirmed the radiological diagnosis. Further, we discuss the imaging findings and the histopathological features of this rare case with a review of the related literature. SAGE Publications 2013-05-31 /pmc/articles/PMC3805425/ /pubmed/24198959 http://dx.doi.org/10.1177/2047981613492532 Text en © 2013 The Foundation Acta Radiologica http://creativecommons.org/licenses/by-nc/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/2.0/), which permits non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Munksgaard, Peter Svenssen
Salkus, Giedrius
Iyer, Victor V
Fisker, Rune Vincents
Mazabraud's syndrome: case report and literature review
title Mazabraud's syndrome: case report and literature review
title_full Mazabraud's syndrome: case report and literature review
title_fullStr Mazabraud's syndrome: case report and literature review
title_full_unstemmed Mazabraud's syndrome: case report and literature review
title_short Mazabraud's syndrome: case report and literature review
title_sort mazabraud's syndrome: case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3805425/
https://www.ncbi.nlm.nih.gov/pubmed/24198959
http://dx.doi.org/10.1177/2047981613492532
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