MRI in autosomal dominant polycystic kidney disease.


Journal

Journal of magnetic resonance imaging : JMRI
ISSN: 1522-2586
Titre abrégé: J Magn Reson Imaging
Pays: United States
ID NLM: 9105850

Informations de publication

Date de publication:
07 2019
Historique:
received: 25 10 2018
revised: 05 12 2018
accepted: 08 12 2018
pubmed: 15 1 2019
medline: 15 8 2020
entrez: 15 1 2019
Statut: ppublish

Résumé

Magnetic resonance imaging (MRI) is increasingly used in autosomal dominant polycystic kidney disease (ADPKD) for diagnosis, classification, assessment of disease progression and treatment response, and for identifying complications. Herein we review the role of MRI in the management of patients with ADPKD. We show how MRI-derived total kidney volume is a biomarker for assessing ADPKD severity and predicting decline in renal function. We also demonstrate the MR appearances of common complications. Level of Evidence: 3 Technical Efficacy Stage: 5 J. Magn. Reson. Imaging 2019;50:41-51.

Identifiants

pubmed: 30637853
doi: 10.1002/jmri.26627
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

41-51

Informations de copyright

© 2019 International Society for Magnetic Resonance in Medicine.

Auteurs

Weiguo Zhang (W)

Department of Radiology, Weill Cornell Medicine, New York, New York, USA.

Jon D Blumenfeld (JD)

Rogosin Institute, and Department of Medicine, Weill Cornell Medicine, New York, New York, USA.

Martin R Prince (MR)

Department of Radiology, Weill Cornell Medicine, New York, New York, USA.
Columbia College of Physicians and Surgeons, New York, New York, USA.

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Classifications MeSH