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Leiomyoma of deep soft tissue mimicking calcific myonecrosis

Leiomyoma of deep soft tissue is an unusual entity reported in less than 60 cases in the English literature. The lesion is now accepted as a rare neoplasm. Leiomyomata of deep soft tissue have been divided into 2 groups, those occurring primarily in women in the retroperitoneum, histologically simil...

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Autores principales: Fitzhugh, Valerie A., Wenokor, Cornelia, Beebe, Kathleen S., Aisner, Seena C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128368/
https://www.ncbi.nlm.nih.gov/pubmed/27920874
http://dx.doi.org/10.1016/j.radcr.2016.08.003
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author Fitzhugh, Valerie A.
Wenokor, Cornelia
Beebe, Kathleen S.
Aisner, Seena C.
author_facet Fitzhugh, Valerie A.
Wenokor, Cornelia
Beebe, Kathleen S.
Aisner, Seena C.
author_sort Fitzhugh, Valerie A.
collection PubMed
description Leiomyoma of deep soft tissue is an unusual entity reported in less than 60 cases in the English literature. The lesion is now accepted as a rare neoplasm. Leiomyomata of deep soft tissue have been divided into 2 groups, those occurring primarily in women in the retroperitoneum, histologically similar to leiomyomata of the uterus, and those occurring equally in both sexes in the somatic deep soft tissues. Irrespective of location, these lesions can demonstrate calcification, and even less commonly ossification. We report a unique case of a leiomyoma of deep soft tissue that mimicked the clinical and radiographic features of calcific myonecrosis, also a rare mass forming soft-tissue lesion. Clinical and radiographic information are often critical in the diagnosis of soft-tissue lesions; however, this case demonstrates that a lesion can deviate from the standard clinical and radiographic interpretations most commonly attributed to it.
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spelling pubmed-51283682016-12-05 Leiomyoma of deep soft tissue mimicking calcific myonecrosis Fitzhugh, Valerie A. Wenokor, Cornelia Beebe, Kathleen S. Aisner, Seena C. Radiol Case Rep Case Report Leiomyoma of deep soft tissue is an unusual entity reported in less than 60 cases in the English literature. The lesion is now accepted as a rare neoplasm. Leiomyomata of deep soft tissue have been divided into 2 groups, those occurring primarily in women in the retroperitoneum, histologically similar to leiomyomata of the uterus, and those occurring equally in both sexes in the somatic deep soft tissues. Irrespective of location, these lesions can demonstrate calcification, and even less commonly ossification. We report a unique case of a leiomyoma of deep soft tissue that mimicked the clinical and radiographic features of calcific myonecrosis, also a rare mass forming soft-tissue lesion. Clinical and radiographic information are often critical in the diagnosis of soft-tissue lesions; however, this case demonstrates that a lesion can deviate from the standard clinical and radiographic interpretations most commonly attributed to it. Elsevier 2016-09-17 /pmc/articles/PMC5128368/ /pubmed/27920874 http://dx.doi.org/10.1016/j.radcr.2016.08.003 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Fitzhugh, Valerie A.
Wenokor, Cornelia
Beebe, Kathleen S.
Aisner, Seena C.
Leiomyoma of deep soft tissue mimicking calcific myonecrosis
title Leiomyoma of deep soft tissue mimicking calcific myonecrosis
title_full Leiomyoma of deep soft tissue mimicking calcific myonecrosis
title_fullStr Leiomyoma of deep soft tissue mimicking calcific myonecrosis
title_full_unstemmed Leiomyoma of deep soft tissue mimicking calcific myonecrosis
title_short Leiomyoma of deep soft tissue mimicking calcific myonecrosis
title_sort leiomyoma of deep soft tissue mimicking calcific myonecrosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128368/
https://www.ncbi.nlm.nih.gov/pubmed/27920874
http://dx.doi.org/10.1016/j.radcr.2016.08.003
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