| Literature DB >> 32798245 |
Christy Cathreen Thomas1, Manisha Jana2, Aditi Sinha1, Arvind Bagga1, Anupama Ramachandran2, Dipin Sudhakaran2, Arun Kumar Gupta2.
Abstract
Renal cysts can be focal or diffuse and unilateral or bilateral. In childhood, most renal cysts are due to hereditary diseases rather than simple cysts or acquired cystic diseases, unlike adults. Inherited cystic diseases can be ciliopathies due to a primary ciliary defect (as in polycystic kidney diseases and nephronophthisis). Acquired causes include obstructive cystic dysplasia, dyselectrolytemia, and acquired cysts in renal replacement therapy. The final diagnosis requires a multispecialty approach, including radiology, pathology, and genetics. Imaging is a very important component in treating patients with cystic renal diseases. This article discusses the ultrasound findings of cystic renal diseases in children, along with a brief discussion of other imaging modalities and a suggested ultrasound reporting format.Entities:
Keywords: autosomal dominant polycystic kidney disease; autosomal recessive polycystic kidney disease; cystic renal disease
Mesh:
Year: 2020 PMID: 32798245 DOI: 10.1002/jum.15435
Source DB: PubMed Journal: J Ultrasound Med ISSN: 0278-4297 Impact factor: 2.153