Literature DB >> 34537211

A case of intramuscular lumbar myxoma: Uncertainty in the preoperative diagnosis of a spinal soft tissue tumour.

A Al Awadhi1, S Benichi2, G Lot2, A Rogers2.   

Abstract

We report an uncommon case of a 76-year-old woman who presented with lower back pain, an intermittent L5 radiculopathy and a right palpable paraspinal mass. Imaging studies revealed a 7-cm lumbar paraspinal pseudo-cystic soft tissue tumour developed in the paravertebral musculature, without a clear radiological diagnosis. Gross total surgical resection was performed, resulting in complete resolution of pain. Histopathological studies revealed an intramuscular (IM) myxoma. With a low positive predictive value of radiological work-up and a poor yield of percutaneous biopsies, surgery remains the mainstay treatment for these rare soft tissue tumours of the lumbar spine. Intramuscular myxomas show excellent postoperative results.
Copyright © 2021 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Diagnosis; Intramuscular myxoma; Lumbar spine; Soft tissue tumor.

Mesh:

Year:  2021        PMID: 34537211     DOI: 10.1016/j.neuchi.2021.08.007

Source DB:  PubMed          Journal:  Neurochirurgie        ISSN: 0028-3770            Impact factor:   1.725


  1 in total

1.  Diagnostic and Therapeutic Pathways of Intramuscular Myxoma.

Authors:  Alonja Reiter; Katharina Trumm; Tobias M Ballhause; Sebastian Weiss; Karl-Heinz Frosch; Alexander Korthaus; Ulrich Bechler; Anna Duprée; Andreas Luebke; Peter Bannas; Carsten W Schlickewei; Matthias H Priemel
Journal:  Diagnostics (Basel)       Date:  2022-06-28
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.