Hajdu-Cheney Syndrome: Report of a Case-Reference-Cited by-同舟云学术

Hajdu-Cheney Syndrome: Report of a Case

Published:2007-11 Issue:6 Volume:10 Page:470-476
ISSN:1093-5266
Container-title:Pediatric and Developmental Pathology
language:en
Short-container-title:Pediatr Dev Pathol

Author:

Ellison Dale A.¹,Ellis Eileen N.²,Kokoska Evan R.³

Affiliation:

1. Departments of Pathology, Arkansas Children's Hospital and University of Arkansas for Medical Sciences, Slot 820, 800 Marshall Street, Little Rock, AR 72202, USA

2. Departments of Nephrology, Arkansas Children's Hospital and University of Arkansas for Medical Sciences, Slot 820, 800 Marshall Street, Little Rock, AR 72202, USA

3. Departments of Surgery, Arkansas Children's Hospital and University of Arkansas for Medical Sciences, Slot 820, 800 Marshall Street, Little Rock, AR 72202, USA

Abstract

Hajdu-Cheney syndrome is a rare disorder characterized by short stature, joint hypermobility, distinctive craniofacial and skull abnormalities, dental anomalies, and acroosteolysis of the distal phalanges. Cystic kidneys have been associated with some cases. We report a case of a 12-year-old girl with renal failure who underwent bilateral nephrectomies. Histopathological examination revealed polycystic kidneys with numerous nodules located throughout the kidney composed of basaloid epithelial cells.

Publisher

SAGE Publications

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.2350/06-07-0132.1

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5. Murphy W, Grignon D, Perlman EJ. Tumors of the Kidney, Bladder, and Related Urinary Structures, 4th ed. Washington, D.C.: American Registry of Pathology, 2004;82–83;123–130;39–46.

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