ホシノ　ジユンイチ   Hoshino Jiyun'ichi   星野　純一    所属   医学部 医学科（東京女子医科大学病院）    職種   教授・基幹分野長
論文種別	総説
言語種別	英語
査読の有無	査読あり
表題	Cystic Kidney Diseases That Require a Differential Diagnosis from Autosomal Dominant Polycystic Kidney Disease (ADPKD).
掲載誌名	正式名：Journal of clinical medicine 略　 称：J Clin Med ISSNコード：20770383/20770383
掲載区分	国外
巻・号・頁	11(21),pp.6528
著者・共著者	Sekine Akinari, Hidaka Sumi, Moriyama Tomofumi, Shikida Yasuto, Shimazu Keiji, Ishikawa Eiji, Uchiyama Kiyotaka, Kataoka Hiroshi, Kawano Haruna, Kurashige Mahiro, Sato Mai, Suwabe Tatsuya, Nakatani Shinya, Otsuka Tadashi, Kai Hirayasu, Katayama Kan, Makabe Shiho, Manabe Shun, Shimabukuro Wataru, Nakanishi Koichi, Nishio Saori, Hattanda Fumihiko, Hanaoka Kazushige, Miura Kenichiro, Hayashi Hiroki, Hoshino Junichi, Tsuchiya Ken, Mochizuki Toshio, Horie Shigeo, Narita Ichiei, Muto Satoru
発行年月	2022/11
概要	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.
DOI	10.3390/jcm11216528
PMID	36362756