TY - JOUR
T1 - Cystic Kidney Diseases That Require a Differential Diagnosis from Autosomal Dominant Polycystic Kidney Disease (ADPKD)
AU - Sekine, Akinari
AU - Hidaka, Sumi
AU - Moriyama, Tomofumi
AU - Shikida, Yasuto
AU - Shimazu, Keiji
AU - Ishikawa, Eiji
AU - Uchiyama, Kiyotaka
AU - Kataoka, Hiroshi
AU - Kawano, Haruna
AU - Kurashige, Mahiro
AU - Sato, Mai
AU - Suwabe, Tatsuya
AU - Nakatani, Shinya
AU - Otsuka, Tadashi
AU - Kai, Hirayasu
AU - Katayama, Kan
AU - Makabe, Shiho
AU - Manabe, Shun
AU - Shimabukuro, Wataru
AU - Nakanishi, Koichi
AU - Nishio, Saori
AU - Hattanda, Fumihiko
AU - Hanaoka, Kazushige
AU - Miura, Kenichiro
AU - Hayashi, Hiroki
AU - Hoshino, Junichi
AU - Tsuchiya, Ken
AU - Mochizuki, Toshio
AU - Horie, Shigeo
AU - Narita, Ichiei
AU - Muto, Satoru
N1 - Publisher Copyright:
© 2022 by the authors.
PY - 2022/11
Y1 - 2022/11
N2 - Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary cystic kidney disease, with patients often having a positive family history that is characterized by a similar phenotype. However, in atypical cases, particularly those in which family history is unclear, a differential diagnosis between ADPKD and other cystic kidney diseases is important. When diagnosing ADPKD, cystic kidney diseases that can easily be excluded using clinical information include: multiple simple renal cysts, acquired cystic kidney disease (ACKD), multilocular renal cyst/multilocular cystic nephroma/polycystic nephroma, multicystic kidney/multicystic dysplastic kidney (MCDK), and unilateral renal cystic disease (URCD). However, there are other cystic kidney diseases that usually require genetic testing, or another means of supplementing clinical information to enable a differential diagnosis of ADPKD. These include autosomal recessive polycystic kidney disease (ARPKD), autosomal dominant tubulointerstitial kidney disease (ADTKD), nephronophthisis (NPH), oral-facial-digital (OFD) syndrome type 1, and neoplastic cystic kidney disease, such as tuberous sclerosis (TSC) and Von Hippel-Lindau (VHL) syndrome. To help physicians evaluate cystic kidney diseases, this article provides a review of cystic kidney diseases for which a differential diagnosis is required for ADPKD.
AB - Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary cystic kidney disease, with patients often having a positive family history that is characterized by a similar phenotype. However, in atypical cases, particularly those in which family history is unclear, a differential diagnosis between ADPKD and other cystic kidney diseases is important. When diagnosing ADPKD, cystic kidney diseases that can easily be excluded using clinical information include: multiple simple renal cysts, acquired cystic kidney disease (ACKD), multilocular renal cyst/multilocular cystic nephroma/polycystic nephroma, multicystic kidney/multicystic dysplastic kidney (MCDK), and unilateral renal cystic disease (URCD). However, there are other cystic kidney diseases that usually require genetic testing, or another means of supplementing clinical information to enable a differential diagnosis of ADPKD. These include autosomal recessive polycystic kidney disease (ARPKD), autosomal dominant tubulointerstitial kidney disease (ADTKD), nephronophthisis (NPH), oral-facial-digital (OFD) syndrome type 1, and neoplastic cystic kidney disease, such as tuberous sclerosis (TSC) and Von Hippel-Lindau (VHL) syndrome. To help physicians evaluate cystic kidney diseases, this article provides a review of cystic kidney diseases for which a differential diagnosis is required for ADPKD.
KW - ADPKD
KW - cystic kidney diseases
KW - differential diagnosis
KW - hereditary
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U2 - 10.3390/jcm11216528
DO - 10.3390/jcm11216528
M3 - Review article
AN - SCOPUS:85141766595
SN - 2077-0383
VL - 11
JO - Journal of Clinical Medicine
JF - Journal of Clinical Medicine
IS - 21
M1 - 6528
ER -