Literature DB >> 11793094

Intracranial aneurysms in a child with autosomal recessive polycystic kidney disease.

M I Lilova1, D L Petkov.   

Abstract

Intracranial aneurysms (ICA) are a well-known feature of autosomal dominant polycystic kidney disease. There is only one report about ICA in an adult patient with autosomal recessive polycystic kidney disease (ARPKD). We observed a 2-year, 6-month old girl with ARPKD and multiple ICA. The family history is negative for kidney disease. The diagnosis of ARPKD was based on the typical findings in ultrasonography and computed tomography. Cystic ectasia of biliary ducts 6.3/4.8 cm in diameter was found in the liver. Arterial hypertension in a range of 140/100-170/120 mm Hg was registered. The child has polyuria, polydipsia and enuresis. Blood urea was 15 mmol/l, creatinine in a range of 120 to 75 micromol/l. One episode of vomiting, dizziness and lethargy was the reason for a brain magnetic resonance imaging. Multiple fusiform and saccular aneurysms in the branches of middle and posterior cerebral arteries were seen bilaterally. The girl is growing well without neurological symptoms during an observation period of 1.5 years. Blood pressure is well controlled with an ACE inhibitor (Enalapril 2.5 mg daily). It was concluded that ICA can be found in patients with ARPKD. Blood pressure control is essential to reduce the risk of intracranial hemorrhage.

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Year:  2001        PMID: 11793094     DOI: 10.1007/s004670100019

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


  11 in total

1.  Hypertension in Autosomal Dominant Polycystic Kidney Disease: A Clinical and Basic Science Perspective.

Authors:  Shobha Ratnam; Surya M Nauli
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2.  Microsurgical management of pediatric intracranial aneurysms.

Authors:  Nader Sanai; Kurtis I Auguste; Michael T Lawton
Journal:  Childs Nerv Syst       Date:  2010-07-13       Impact factor: 1.475

Review 3.  Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes.

Authors:  Rainer Büscher; Anja K Büscher; Stefanie Weber; Julia Mohr; Bianca Hegen; Udo Vester; Peter F Hoyer
Journal:  Pediatr Nephrol       Date:  2013-10-10       Impact factor: 3.714

Review 4.  Polycystic liver diseases.

Authors:  P Onori; A Franchitto; R Mancinelli; G Carpino; D Alvaro; H Francis; G Alpini; E Gaudio
Journal:  Dig Liver Dis       Date:  2010-02-06       Impact factor: 4.088

5.  A 4-year-old girl with autosomal dominant polycystic kidney disease complicated by a ruptured intracranial aneurysm.

Authors:  Satomi Kubo; Mitsuru Nakajima; Kazuyoshi Fukuda; Misato Nobayashi; Toshisuke Sakaki; Katsuya Aoki; Yoshihiko Hirao; Akira Yoshioka
Journal:  Eur J Pediatr       Date:  2004-08-19       Impact factor: 3.183

6.  Polycystin-2 expression is regulated by a PC2-binding domain in the intracellular portion of fibrocystin.

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Journal:  J Biol Chem       Date:  2008-09-09       Impact factor: 5.157

7.  Fibrocystin/polyductin modulates renal tubular formation by regulating polycystin-2 expression and function.

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Journal:  J Am Soc Nephrol       Date:  2008-01-30       Impact factor: 10.121

Review 8.  Vascular complications in autosomal dominant polycystic kidney disease.

Authors:  Ronald D Perrone; Adel M Malek; Terry Watnick
Journal:  Nat Rev Nephrol       Date:  2015-08-11       Impact factor: 28.314

9.  The mechanosensory role of primary cilia in vascular hypertension.

Authors:  Surya M Nauli; Xingjian Jin; Beerend P Hierck
Journal:  Int J Vasc Med       Date:  2011-06-16

10.  Polycystic kidney disease: inheritance, pathophysiology, prognosis, and treatment.

Authors:  Christian R Halvorson; Matthew S Bremmer; Stephen C Jacobs
Journal:  Int J Nephrol Renovasc Dis       Date:  2010-06-24
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