Ferumoxytol-enhanced MR imaging for differentiating intrapancreatic splenules from other tumors
| Autor: | L. L. Bergmann, E. Winslow, M. R. Muehler, Scott B. Reeder, Victoria R. Rendell |
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| Rok vydání: | 2020 |
| Předmět: |
medicine.medical_specialty
Splenule Urology Fat suppression Contrast Media Neuroendocrine tumor Neoplasms Internal medicine medicine Humans Radiology Nuclear Medicine and imaging Magnetic resonance imaging (MRI) Pancreatic lesion Pancreas Retrospective Studies Ferumoxytol Radiological and Ultrasound Technology business.industry Gastroenterology Retrospective cohort study Hepatology Magnetic Resonance Imaging Mr imaging Ferrosoferric Oxide Diffusion Magnetic Resonance Imaging Ultra-small super paramagnetic iron oxides (USPIO) medicine.anatomical_structure Splenic Tissue Radiology business |
| Zdroj: | Abdominal Radiology (New York) |
| ISSN: | 2366-0058 2366-004X |
| DOI: | 10.1007/s00261-020-02883-y |
| Popis: | Objectives Ferumoxytol is an ultra-small superparamagnetic iron oxide (USPIO) agent that is taken up by splenic tissue. This study describes our initial institutional experience of ferumoxytol-enhanced MRI (feMRI) for differentiating intrapancreatic splenules (IPS) from other pancreatic lesions. Methods In this retrospective study, patients with computed tomographic imaging that identified small enhancing lesions in the tail of the pancreas subsequently underwent feMRI for further characterization. The feMRI protocol included T2-weighted (T2w) imaging with and without fat suppression (FS), R2* mapping, diffusion-weighted imaging (DWI), and T1-weighted (T1w) imaging with FS, prior to contrast injection. Immediately after slow intravenous infusion with 3 mg/kg body weight ferumoxytol, T1w was repeated. Delayed imaging with all sequences were obtained 24–72 h after ferumoxytol administration. Results Seven patients underwent feMRI. In two patients, the pancreatic lesions were presumed as pancreatic neuroendocrine tumor (PNET) from feMRI and in the remaining 5 IPS. One of the two patients with PNET was symptomatic for NET. In another symptomatic patient with pathologically proven duodenal NET and suspected PNET, the pancreatic lesion was proven to be an IPS on feMRI. IPS demonstrated strong negative enhancement in feMRI on T2w and increased R2* values consistent with splenic tissue, while the presumed PNETs did not enhance. T2w FS was helpful on the pre-contrast images to identify IPS, while R2* did on post-contrast images. Neither DWI nor T1w contributed to differentiating PNETs from IPS. Conclusions This study demonstrates the potential utility of feMRI as a helpful adjunct diagnostic tool for differentiating IPS from other pancreatic lesions. Further studies in larger patient cohorts are needed. |
| Databáze: | OpenAIRE |
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