Literature DB >> 27153791

Taxonomy and Imaging Manifestations of Systemic Amyloidosis.

Naoki Takahashi1, James Glockner2, Benjamin M Howe2, Robert P Hartman2, Akira Kawashima3.   

Abstract

Amyloidosis is a heterogeneous group of disorders that are characterized by extracellular deposition of misfolded and aggregated autologous proteins leading to organ dysfunction. Amyloid deposits produce diverse clinical syndromes depending on their type, location, and the amount of deposition. Clinical and imaging features of amyloidosis in various organ systems are described.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Amyloidosis; Computed tomography; Heart; Joint; Lung; MR imaging; Urinary tract

Mesh:

Year:  2016        PMID: 27153791     DOI: 10.1016/j.rcl.2015.12.012

Source DB:  PubMed          Journal:  Radiol Clin North Am        ISSN: 0033-8389            Impact factor:   2.303


  2 in total

1.  [18F]Florbetaben PET-CT confirms AL amyloidosis in a patient with Waldenström's Macroglobulinemia.

Authors:  Thomas A Fox; Michael Lunn; Ashutosh Wechalekar; Jamshed Bomanji; Simon Wan; Shirley D'Sa
Journal:  Haematologica       Date:  2018-04-12       Impact factor: 9.941

Review 2.  Nodular pulmonary amyloidosis: a complex disease with malignancy association.

Authors:  Jacob M Core; Ali A Alsaad; Liuyan Jiang; Neal M Patel
Journal:  BMJ Case Rep       Date:  2017-10-15
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.