Literature DB >> 33786104

Aortic Dissection in Familial Patients with Autosomal Dominant Polycystic Kidney Disease.

Yu Inaba1, Motohiko Osako1, Michiko Aoki1, Mio Kasai1, Kentaro Yamabe1.   

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is the most common congenital kidney disease. However, reports on occasional cases of aortic dissection in PKD familial patients remain scarce. Herein, we describe rare aortic dissection cases in PKD familial patients (i.e., mother and daughter) and our successful treatment experience. The mother (84 years old) and daughter (53 years old) had a referral to us to treat type A acute aortic dissection. We performed emergency surgery and successfully treated the patients with an artificial graft. For comprehensive evaluation and treatment, ADPKD patients and their families should be screened for aortic diseases.
© 2021 The Editorial Committee of Annals of Vascular Diseases.

Entities:  

Keywords:  ADPKD; aortic dissection

Year:  2021        PMID: 33786104      PMCID: PMC7991707          DOI: 10.3400/avd.cr.20-00149

Source DB:  PubMed          Journal:  Ann Vasc Dis        ISSN: 1881-641X


  8 in total

1.  Epidemiological study of kidney survival in autosomal dominant polycystic kidney disease.

Authors:  Robert W Schrier; Kimberly K McFann; Ann M Johnson
Journal:  Kidney Int       Date:  2003-02       Impact factor: 10.612

Review 2.  Is Regular Screening for Intracranial Aneurysm Necessary in Patients with Autosomal Dominant Polycystic Kidney Disease? A Systematic Review and Meta-analysis.

Authors:  Zien Zhou; Ying Xu; Candice Delcourt; Jiehui Shan; Qiang Li; Jianrong Xu; Maree L Hackett
Journal:  Cerebrovasc Dis       Date:  2017-05-13       Impact factor: 2.762

3.  Mitral valve prolapse and mitral regurgitation are common in patients with polycystic kidney disease type 1.

Authors:  A Lumiaho; R Ikäheimo; R Miettinen; L Niemitukia; T Laitinen; A Rantala; E Lampainen; M Laakso; J Hartikainen
Journal:  Am J Kidney Dis       Date:  2001-12       Impact factor: 8.860

Review 4.  Autosomal dominant polycystic kidney disease.

Authors:  Emilie Cornec-Le Gall; Ahsan Alam; Ronald D Perrone
Journal:  Lancet       Date:  2019-02-25       Impact factor: 79.321

Review 5.  Aortic dissection in patients with autosomal dominant polycystic kidney disease: a series of two cases and a review of the literature.

Authors:  Angelo Silverio; Costantina Prota; Marco Di Maio; Maria Vincenza Polito; Francesco Maria Cogliani; Rodolfo Citro; Alberto Gigantino; Severino Iesu; Federico Piscione
Journal:  Nephrology (Carlton)       Date:  2015-04       Impact factor: 2.506

6.  Expression of components of the renin-angiotensin system in autosomal recessive polycystic kidney disease.

Authors:  Mahmoud Loghman-Adham; Carlos E Soto; Tadashi Inagami; Cirilo Sotelo-Avila
Journal:  J Histochem Cytochem       Date:  2005-05-06       Impact factor: 2.479

7.  Pathogenic sequence for dissecting aneurysm formation in a hypomorphic polycystic kidney disease 1 mouse model.

Authors:  Sabrine Hassane; Nanna Claij; Irma S Lantinga-van Leeuwen; J Conny Van Munsteren; Natascha Van Lent; Roeland Hanemaaijer; Martijn H Breuning; Dorien J M Peters; Marco C DeRuiter
Journal:  Arterioscler Thromb Vasc Biol       Date:  2007-07-26       Impact factor: 8.311

8.  Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1.

Authors:  D Ravine; R N Gibson; R G Walker; L J Sheffield; P Kincaid-Smith; D M Danks
Journal:  Lancet       Date:  1994-04-02       Impact factor: 79.321

  8 in total

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