Literature DB >> 32040628

The "salt and pepper" pattern on renal ultrasound in a group of children with molecular-proven diagnosis of ciliopathy-related renal diseases.

Pauline Iorio1, Laurence Heidet2,3, Caroline Rutten4, Nicolas Garcelon5, Marie-Pierre Audrézet6, Vincent Morinière7, Nathalie Boddaert4,5,8,9,10, Rémi Salomon2,5,8, Laureline Berteloot4,9.   

Abstract

BACKGROUND: While typical ultrasound patterns of ciliopathy-related cystic kidney diseases have been described in children, ultrasound findings can overlap between different diseases and atypical patterns exist. In this study, we assessed the presence of the "salt and pepper" pattern in different renal ciliopathies and looked for additional ultrasound features.
METHODS: This single-center, retrospective study included all patients with a molecular-proven diagnosis of renal ciliopathy, referred to our center between 2007 and 2017. Images from the first and follow-up ultrasound exams were reviewed. Basic ultrasound features were grouped into patterns and compared to genetic diagnoses. The "salt and pepper" aspect was described as enlarged kidneys with heterogeneous, increased parenchymal echogenicity.
RESULTS: A total of 41 children with 5 different renal ciliopathies were included (61% male; median age, 6 years [range, 3 days to 17 years]). The "salt and pepper" pattern was present in 14/15 patients with an autosomal recessive polycystic kidney disease (ARPKD). A similar pattern was found in 1/4 patients with an autosomal dominant polycystic kidney disease and in 1/11 patients with HNF1B mutation. Additional signs found were areas of cortical sparing, comet-tail artifacts, and color comet-tail artifacts.
CONCLUSION: Although the "salt and pepper" ultrasound pattern is predominantly found in ARPKD, it may be detected in other ciliopathies. The color comet-tail artifact is an interesting sign when suspecting a renal ciliopathy in case of enlarged hyperechoic kidneys with no detectable microcysts on B-mode grayscale ultrasound.

Entities:  

Keywords:  Cystic disease; Molecular genetics; Renal Ciliopathies; Ultrasound

Mesh:

Year:  2020        PMID: 32040628     DOI: 10.1007/s00467-020-04480-z

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  26 in total

Review 1.  Autosomal dominant polycystic kidney disease: the changing face of clinical management.

Authors:  Albert C M Ong; Olivier Devuyst; Bertrand Knebelmann; Gerd Walz
Journal:  Lancet       Date:  2015-05-16       Impact factor: 79.321

Review 2.  Clinical Significance of US Artifacts.

Authors:  Michael Baad; Zheng Feng Lu; Ingrid Reiser; David Paushter
Journal:  Radiographics       Date:  2017-08-04       Impact factor: 5.333

Review 3.  Cystic diseases of the kidney: molecular biology and genetics.

Authors:  Constantinos Deltas; Gregory Papagregoriou
Journal:  Arch Pathol Lab Med       Date:  2010-04       Impact factor: 5.534

Review 4.  Motile and non-motile cilia in human pathology: from function to phenotypes.

Authors:  Hannah M Mitchison; Enza Maria Valente
Journal:  J Pathol       Date:  2017-01       Impact factor: 7.996

Review 5.  Diagnosis and screening of autosomal dominant polycystic kidney disease.

Authors:  York Pei; Terry Watnick
Journal:  Adv Chronic Kidney Dis       Date:  2010-03       Impact factor: 3.620

Review 6.  Imaging and classification of congenital cystic renal diseases.

Authors:  Fred E Avni; Catherine Garel; Marie Cassart; Nicky D'Haene; Michele Hall; Michael Riccabona
Journal:  AJR Am J Roentgenol       Date:  2012-05       Impact factor: 3.959

Review 7.  Role of primary cilia in the pathogenesis of polycystic kidney disease.

Authors:  Bradley K Yoder
Journal:  J Am Soc Nephrol       Date:  2007-04-11       Impact factor: 10.121

8.  Rationale, design and objectives of ARegPKD, a European ARPKD registry study.

Authors:  Kathrin Ebner; Markus Feldkoetter; Gema Ariceta; Carsten Bergmann; Reinhard Buettner; Anke Doyon; Ali Duzova; Heike Goebel; Dieter Haffner; Barbara Hero; Bernd Hoppe; Thomas Illig; Augustina Jankauskiene; Norman Klopp; Jens König; Mieczyslaw Litwin; Djalila Mekahli; Bruno Ranchin; Anja Sander; Sara Testa; Lutz Thorsten Weber; Dorota Wicher; Ayse Yuzbasioglu; Klaus Zerres; Jörg Dötsch; Franz Schaefer; Max Christoph Liebau
Journal:  BMC Nephrol       Date:  2015-02-18       Impact factor: 2.388

9.  International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people.

Authors:  Charlotte Gimpel; Carsten Bergmann; Detlef Bockenhauer; Luc Breysem; Melissa A Cadnapaphornchai; Metin Cetiner; Jan Dudley; Francesco Emma; Martin Konrad; Tess Harris; Peter C Harris; Jens König; Max C Liebau; Matko Marlais; Djalila Mekahli; Alison M Metcalfe; Jun Oh; Ronald D Perrone; Manish D Sinha; Andrea Titieni; Roser Torra; Stefanie Weber; Paul J D Winyard; Franz Schaefer
Journal:  Nat Rev Nephrol       Date:  2019-11       Impact factor: 28.314

Review 10.  ARPKD and early manifestations of ADPKD: the original polycystic kidney disease and phenocopies.

Authors:  Carsten Bergmann
Journal:  Pediatr Nephrol       Date:  2014-03-01       Impact factor: 3.714

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  2 in total

Review 1.  Autosomal Recessive Polycystic Kidney Disease-The Clinical Aspects and Diagnostic Challenges.

Authors:  Dorota Wicher; Łukasz Obrycki; Irena Jankowska
Journal:  J Pediatr Genet       Date:  2020-07-29

2.  Challenging Disease Ontology by Instances of Atypical PKHD1 and PKD1 Genetics.

Authors:  Jonathan de Fallois; Ria Schönauer; Johannes Münch; Mato Nagel; Bernt Popp; Jan Halbritter
Journal:  Front Genet       Date:  2021-06-25       Impact factor: 4.599

  2 in total

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