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Congenital Thoracic Ectopic Kidney associated with Diaphragmatic Hernia in a 15-month-old Boy
Journal of the Korean Society of Pediatric Nephrology ; : 106-110, 2014.
Article in English | WPRIM | ID: wpr-223756
ABSTRACT
Congenital thoracic ectopic kidney is a very rare developmental disorder and the rarest type of ectopic kidney. This condition is usually asymptomatic and detected incidentally on routine chest radiography. Most cases of thoracic ectopic kidney develop in adulthood and during the neonatal period, and congenital thoracic ectopic kidney rarely develops in children. Most patients are asymptomatic, and the treatment depends on the diagnosis. Herein, we report a rare case of ectopic thoracic kidney associated with a diaphragmatic hernia in a 15-month-old male infant, who presented with periodic severe irritability. The thoracic ectopic kidney was detected as a mass in the right base of the chest on routine chest radiography.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Thorax / Radiography / Diagnosis / Hernia, Diaphragmatic / Kidney Type of study: Diagnostic study Limits: Child / Humans / Infant / Male Language: English Journal: Journal of the Korean Society of Pediatric Nephrology Year: 2014 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Thorax / Radiography / Diagnosis / Hernia, Diaphragmatic / Kidney Type of study: Diagnostic study Limits: Child / Humans / Infant / Male Language: English Journal: Journal of the Korean Society of Pediatric Nephrology Year: 2014 Type: Article