Magnetic resonance imaging in the assessment of pancreatic cancer with quantitative parameter extraction by means of dynamic contrast-enhanced magnetic resonance imaging, diffusion kurtosis imaging and intravoxel incoherent motion diffusion-weighted imaging.

diffusion magnetic resonance imaging pancreatic cancer perfusion

Journal

Therapeutic advances in gastroenterology
ISSN: 1756-283X
Titre abrégé: Therap Adv Gastroenterol
Pays: England
ID NLM: 101478893

Informations de publication

Date de publication:
2020
Historique:
received: 19 06 2019
accepted: 07 10 2019
entrez: 6 6 2020
pubmed: 6 6 2020
medline: 6 6 2020
Statut: epublish

Résumé

Despite great technical advances in imaging, such as multidetector computed tomography and magnetic resonance imaging (MRI), diagnosing pancreatic solid lesions correctly remains challenging, due to overlapping imaging features with benign lesions. We wanted to evaluate functional MRI to differentiate pancreatic tumors, peritumoral inflammatory tissue, and normal pancreatic parenchyma by means of dynamic contrast-enhanced MRI (DCE-MRI)-, diffusion kurtosis imaging (DKI)-, and intravoxel incoherent motion model (IVIM) diffusion-weighted imaging (DWI)-derived parameters. We retrospectively analyzed 24 patients, each with histopathological diagnosis of pancreatic tumor, and 24 patients without pancreatic lesions. Functional MRI was acquired using a 1.5 MR scanner. Peritumoral inflammatory tissue was assessed by drawing regions of interest on the tumor contours. DCE-MRI, IVIM and DKI parameters were extracted. Nonparametric tests and receiver operating characteristic (ROC) curves were calculated. There were statistically significant differences in median values among the three groups observed by Kruskal-Wallis test for the DKI mean diffusivity (MD), IVIM perfusion fraction (fp) and IVIM tissue pure diffusivity (Dt). MD had the best results to discriminate normal pancreas plus peritumoral inflammatory tissue Diffusion parameters, mainly MD by DKI, could be helpful for the differentiation of normal pancreatic parenchyma, perilesional inflammation, and pancreatic tumor.

Sections du résumé

BACKGROUND BACKGROUND
Despite great technical advances in imaging, such as multidetector computed tomography and magnetic resonance imaging (MRI), diagnosing pancreatic solid lesions correctly remains challenging, due to overlapping imaging features with benign lesions. We wanted to evaluate functional MRI to differentiate pancreatic tumors, peritumoral inflammatory tissue, and normal pancreatic parenchyma by means of dynamic contrast-enhanced MRI (DCE-MRI)-, diffusion kurtosis imaging (DKI)-, and intravoxel incoherent motion model (IVIM) diffusion-weighted imaging (DWI)-derived parameters.
METHODS METHODS
We retrospectively analyzed 24 patients, each with histopathological diagnosis of pancreatic tumor, and 24 patients without pancreatic lesions. Functional MRI was acquired using a 1.5 MR scanner. Peritumoral inflammatory tissue was assessed by drawing regions of interest on the tumor contours. DCE-MRI, IVIM and DKI parameters were extracted. Nonparametric tests and receiver operating characteristic (ROC) curves were calculated.
RESULTS RESULTS
There were statistically significant differences in median values among the three groups observed by Kruskal-Wallis test for the DKI mean diffusivity (MD), IVIM perfusion fraction (fp) and IVIM tissue pure diffusivity (Dt). MD had the best results to discriminate normal pancreas plus peritumoral inflammatory tissue
CONCLUSIONS CONCLUSIONS
Diffusion parameters, mainly MD by DKI, could be helpful for the differentiation of normal pancreatic parenchyma, perilesional inflammation, and pancreatic tumor.

Identifiants

pubmed: 32499833
doi: 10.1177/1756284819885052
pii: 10.1177_1756284819885052
pmc: PMC7243396
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1756284819885052

Informations de copyright

© The Author(s), 2020.

Déclaration de conflit d'intérêts

Conflict of interest statement: Robert Grimm is an employee of Siemens Healthcare.

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Auteurs

Vincenza Granata (V)

Radiology Unit, 'Istituto Nazionale Tumori - IRCCS - Fondazione G. Pascale', Naples, Italy.

Roberta Fusco (R)

Department of Radiology, Istituto Nazionale Tumori Fondazione G. Pascale, via Mariano Semmola, Naples 80131, Italy.

Mario Sansone (M)

Department of Electrical Engineering and Information Technologies (DIETI), University of Naples Federico II, Naples, Italy.

Roberto Grassi (R)

Radiology Unit, Università della Campania Luigi Vanvitelli, Naples, Italy.

Francesca Maio (F)

Radiology Unit, University of Naples Federico II, Naples, Italy.

Raffaele Palaia (R)

Hepatobiliary Surgical Oncology Unit, 'Istituto Nazionale Tumori - IRCCS - Fondazione G. Pascale', Naples, Italy.

Fabiana Tatangelo (F)

Diagnostic Pathology Unit, 'Istituto Nazionale Tumori - IRCCS - Fondazione G. Pascale', Naples, Italy.

Gerardo Botti (G)

Diagnostic Pathology Unit, 'Istituto Nazionale Tumori - IRCCS - Fondazione G. Pascale', Naples, Italy.

Robert Grimm (R)

Siemens Healthcare GmbH, Erlangen, Bayern, Germany.

Steven Curley (S)

Department of Surgery, Baylor College of Medicine, Houston, TX, USA.

Antonio Avallone (A)

Abdominal Oncology Unit, 'Istituto Nazionale Tumori - IRCCS - Fondazione G. Pascale', Naples, Italy.

Francesco Izzo (F)

Hepatobiliary Surgical Oncology Unit, 'Istituto Nazionale Tumori - IRCCS - Fondazione G. Pascale', Naples, Italy.

Antonella Petrillo (A)

Radiology Unit, 'Istituto Nazionale Tumori - IRCCS - Fondazione G. Pascale', Naples, Italy.

Classifications MeSH