4.3 Article

Steady-state ferumoxytol-enhanced MRI: early observations in benign abdominal organ masses and clinical implications

Journal

ABDOMINAL RADIOLOGY
Volume 47, Issue 1, Pages 460-470

Publisher

SPRINGER
DOI: 10.1007/s00261-021-03271-w

Keywords

Ferumoxytol; Ultra-small super paramagnetic iron oxide; Contrast media; Steady-state; Magnetic resonance imaging; Renal insuffiency

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The study on the off-label use of ferumoxytol as a vascular MR imaging agent showed that it plays an important role in the detection and characterization of benign abdominal mass lesions. The enhancement characteristics of ferumoxytol helped increase diagnostic confidence for benign masses and were consistent with other imaging modalities and follow-up results.
Introduction The off-label use of ferumoxytol as a vascular MR imaging agent is growing rapidly. However, the properties of ferumoxytol suggest that it may play an important role in the detection and characterization of abdominal mass lesions. Methods Thirty-six patients with benign abdominal mass lesions who underwent MR angiography with ferumoxytol also had T2-weighted HASTE imaging and fat-suppressed 3D T1-weighted imaging. The T1 and T2 enhancement characteristics of the lesions were analyzed and correlated with other imaging modalities and/or surgical findings and/or clinical follow-up. Results In all patients with benign masses in the liver (n = 22 patients), spleen (n = 6 patients), kidneys (n = 33 patients), adrenal (n = 2 patients) and pancreas (n = 4 patients), based on the enhancement characteristics with ferumoxytol, readers were confident of the benign nature of the lesions and their conclusions were consistent with correlative imaging, tissue sampling and follow-up. One patient with a suspicious enhancing 2F Bosniak renal cyst had renal cell carcinoma confirmed on biopsy. Conclusion Ferumoxytol-enhanced MRI can increase diagnostic confidence for benign abdominal masses and can increase the conspicuity of mass lesions, relative to unenhanced MRI. Graphic Abstract

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