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Lumbar paraspinal atypical spindle cell/pleomorphic lipomatous tumor: A report of a rare case
The atypical spindle cell/pleomorphic lipomatous tumor (ASPLT) was classified as a new tumor by the World Health Organization (WHO) in 2020. The tumor is benign and commonly occurs in the limbs. Paraspinal presentations are rare. A 38‐year‐old man presented at our clinic complaining of sudden onset...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883842/ https://www.ncbi.nlm.nih.gov/pubmed/36726691 http://dx.doi.org/10.1002/ccr3.6868 |
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author | Cheng, Yu‐Wen Chen, Yang‐Yi Kuo, Chao‐Hung Liao, Wei‐Chuan Kwan, Aij‐Lie |
author_facet | Cheng, Yu‐Wen Chen, Yang‐Yi Kuo, Chao‐Hung Liao, Wei‐Chuan Kwan, Aij‐Lie |
author_sort | Cheng, Yu‐Wen |
collection | PubMed |
description | The atypical spindle cell/pleomorphic lipomatous tumor (ASPLT) was classified as a new tumor by the World Health Organization (WHO) in 2020. The tumor is benign and commonly occurs in the limbs. Paraspinal presentations are rare. A 38‐year‐old man presented at our clinic complaining of sudden onset back pain. No neurological deficit was found. The magnetic resonance imaging (MRI) revealed a well‐defined heterogeneous mass in the left psoas muscle, from L1 to L3 extending over the L1 and L2 neuroforamen. The tumor was totally excised. Pathology led to an ASPLT diagnosis. Clinical symptoms improved and there was no postsurgical neurological deficit. This case of ASPLT, located in an uncommon location and present an unusual cluster of symptoms, could be treated by surgical excision, usually the first‐treatment strategy. Totally, removal was achieved because there was a clear morphological margin. The risk of metastatic dissemination was minimal, though there remains a nonnegligible risk of local recurrence. |
format | Online Article Text |
id | pubmed-9883842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98838422023-01-31 Lumbar paraspinal atypical spindle cell/pleomorphic lipomatous tumor: A report of a rare case Cheng, Yu‐Wen Chen, Yang‐Yi Kuo, Chao‐Hung Liao, Wei‐Chuan Kwan, Aij‐Lie Clin Case Rep Case Report The atypical spindle cell/pleomorphic lipomatous tumor (ASPLT) was classified as a new tumor by the World Health Organization (WHO) in 2020. The tumor is benign and commonly occurs in the limbs. Paraspinal presentations are rare. A 38‐year‐old man presented at our clinic complaining of sudden onset back pain. No neurological deficit was found. The magnetic resonance imaging (MRI) revealed a well‐defined heterogeneous mass in the left psoas muscle, from L1 to L3 extending over the L1 and L2 neuroforamen. The tumor was totally excised. Pathology led to an ASPLT diagnosis. Clinical symptoms improved and there was no postsurgical neurological deficit. This case of ASPLT, located in an uncommon location and present an unusual cluster of symptoms, could be treated by surgical excision, usually the first‐treatment strategy. Totally, removal was achieved because there was a clear morphological margin. The risk of metastatic dissemination was minimal, though there remains a nonnegligible risk of local recurrence. John Wiley and Sons Inc. 2023-01-28 /pmc/articles/PMC9883842/ /pubmed/36726691 http://dx.doi.org/10.1002/ccr3.6868 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Report Cheng, Yu‐Wen Chen, Yang‐Yi Kuo, Chao‐Hung Liao, Wei‐Chuan Kwan, Aij‐Lie Lumbar paraspinal atypical spindle cell/pleomorphic lipomatous tumor: A report of a rare case |
title | Lumbar paraspinal atypical spindle cell/pleomorphic lipomatous tumor: A report of a rare case |
title_full | Lumbar paraspinal atypical spindle cell/pleomorphic lipomatous tumor: A report of a rare case |
title_fullStr | Lumbar paraspinal atypical spindle cell/pleomorphic lipomatous tumor: A report of a rare case |
title_full_unstemmed | Lumbar paraspinal atypical spindle cell/pleomorphic lipomatous tumor: A report of a rare case |
title_short | Lumbar paraspinal atypical spindle cell/pleomorphic lipomatous tumor: A report of a rare case |
title_sort | lumbar paraspinal atypical spindle cell/pleomorphic lipomatous tumor: a report of a rare case |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883842/ https://www.ncbi.nlm.nih.gov/pubmed/36726691 http://dx.doi.org/10.1002/ccr3.6868 |
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