In vivo characterisation of soft tissue tumours by 1.5-T proton MR spectroscopy
- PMID: 22138734
- DOI: 10.1007/s00330-011-2350-9
In vivo characterisation of soft tissue tumours by 1.5-T proton MR spectroscopy
Abstract
Objectives: To determine whether proton magnetic resonance spectroscopy (1H-MRS) can help differentiate between benign and malignant soft tissue lesions, and to assess if there is a correlation between 1H-MRS data and the mitotic index.
Methods: MR measurements were performed in 43 patients with soft tissue tumours >15 mm in diameter. Six cases were excluded for technical failure. Examinations were performed at 1.5 T using a single-voxel point resolved spectroscopy sequence (PRESS) with TR/TE = 2000/150 ms. The volume of interest was positioned within the lesion avoiding inclusion of necrotic regions. In all patients, a histological diagnosis was obtained and the corresponding mitotic index was also computed. 1H-MRS results and histopathological findings were compared using the chi-squared test and correlation coefficient.
Results: Choline was detected in 18/19 patients with malignant tumours and in 3/18 patients with benign lesions. The three benign lesions included one desmoid tumour, one ossificans myositis and one eccrine spiradenoma. Choline was not detected in 15 patients with benign lesions or in one patient with dermatofibrosarcoma protuberans. Resulting 1H-MRS sensitivity and specificity were 95% and 83% respectively.
Conclusions: Absence of choline peak is highly predictive of benign tumours suggesting that 1H-MRS can help to differentiate malignant from benign tumours.
Key points: • 1H-MRS may allow differentiation between benign and malignant soft tissue lesions • Absence of choline peak is highly predictive of benign soft tissue lesions • Malignant tumours with a mitotic index >2/10 HPF had a positive choline peak • A choline peak may still be identified in some benign tumours.
Similar articles
-
Characterization of bone and soft-tissue tumors with in vivo 1H MR spectroscopy: initial results.Radiology. 2004 Aug;232(2):599-605. doi: 10.1148/radiol.2322031441. Radiology. 2004. PMID: 15286325
-
Preliminary study of 3T 1H MR spectroscopy in bone and soft tissue tumors.Chin Med J (Engl). 2009 Jan 5;122(1):39-43. Chin Med J (Engl). 2009. PMID: 19187615
-
Study of single voxel 1H MR spectroscopy of bone tumors: differentiation of benign from malignant tumors.Eur J Radiol. 2013 Dec;82(12):2124-8. doi: 10.1016/j.ejrad.2011.11.033. Epub 2011 Dec 12. Eur J Radiol. 2013. PMID: 22169357
-
Molecular characterization of musculoskeletal tumors by proton MR spectroscopy.Semin Musculoskelet Radiol. 2007 Sep;11(3):240-5. doi: 10.1055/s-2008-1038313. Semin Musculoskelet Radiol. 2007. PMID: 18260034 Review.
-
In vivo proton magnetic resonance spectroscopy of breast lesions: an update.Breast Cancer Res Treat. 2007 Sep;104(3):249-55. doi: 10.1007/s10549-006-9412-8. Epub 2006 Oct 19. Breast Cancer Res Treat. 2007. PMID: 17051424 Review.
Cited by
-
Characterisation of musculoskeletal tumours by multivoxel proton MR spectroscopy.Skeletal Radiol. 2017 Apr;46(4):483-495. doi: 10.1007/s00256-017-2573-1. Epub 2017 Feb 11. Skeletal Radiol. 2017. PMID: 28188338
-
MR Spectra of Normal Adult Testes and Variations with Age: Preliminary Observations.Eur Radiol. 2016 Jul;26(7):2261-7. doi: 10.1007/s00330-015-4055-y. Epub 2015 Oct 16. Eur Radiol. 2016. PMID: 26474986
-
Advanced magnetic resonance imaging (MRI) of soft tissue tumors: techniques and applications.Radiol Med. 2019 Apr;124(4):243-252. doi: 10.1007/s11547-019-01035-7. Epub 2019 Apr 4. Radiol Med. 2019. PMID: 30949892 Review.
-
Proton magnetic resonance spectroscopy in oncology: the fingerprints of cancer?Diagn Interv Radiol. 2016 Jan-Feb;22(1):75-89. doi: 10.5152/dir.2015.15009. Diagn Interv Radiol. 2016. PMID: 26712681 Free PMC article.
-
Influence of calcium on choline measurements by 1H MR spectroscopy of thigh muscles.Eur Radiol. 2014 Jun;24(6):1309-19. doi: 10.1007/s00330-014-3131-z. Epub 2014 Mar 16. Eur Radiol. 2014. PMID: 24633428
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources