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Development of a risk assessment model to differentiate malignant and benign musculoskeletal soft‐tissue masses on magnetic resonance imaging
Author(s) -
Obaid Haron,
Vassos Nicholas,
Adams Scott J,
Bryce Rhonda,
Donuru Achala,
Sinclair Nicolette
Publication year - 2020
Publication title -
journal of medical imaging and radiation oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.31
H-Index - 43
eISSN - 1754-9485
pISSN - 1754-9477
DOI - 10.1111/1754-9485.12981
Subject(s) - medicine , malignancy , soft tissue , univariate analysis , neurovascular bundle , biopsy , radiology , magnetic resonance imaging , deep fascia , logistic regression , fascia , pathology , multivariate analysis
This study aimed to develop a risk stratification model to differentiate benign and malignant MRI‐imaged musculoskeletal soft‐tissue tumours, informing decisions surrounding biopsy and follow‐up imaging. Methods Imaging of patients who underwent MRI and subsequent biopsy to evaluate a soft‐tissue mass was retrospectively reviewed. Features analysed included patient age; tumour size; shape; margins; enhancement pattern; signal intensity pattern; deep fascia, neurovascular bundle, bone and joint involvement; and the presence of necrosis, haemorrhage, oedema and intralesional fat. Univariate comparisons, by final histopathological status, employed t ‐tests and chi‐square tests, followed by simple and multiple logistic regressions. Variables included in the final multiple regression model were used to define a three‐level risk stratification strategy. Results One‐hundred and ten patients were included in the analysis. Univariate relationships were identified between malignancy and age, tumour size, deep fascia involvement, neurovascular involvement, necrosis, haemorrhage, oedema and heterogeneous enhancement (all P < 0.01). Final multiple regression modelling included size, enhancement and oedema. Thirty of 40 (75%) tumours >5 cm with surrounding oedema (‘high risk’) were malignant, 13 of 47 (28%) tumours with one or more of tumour size >5 cm, surrounding oedema or heterogeneous enhancement (‘moderate risk’) were malignant, and none of the 16 tumours ≤5 cm with the absence of surrounding oedema and heterogeneous enhancement (‘low risk’) were malignant. Conclusions A model including tumour size, enhancement and oedema has potential to stratify soft‐tissue tumours into high‐, intermediate‐ and low‐risk categories; this may inform decisions surrounding biopsy and follow‐up imaging.