2004, Number 2
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Gac Med Mex 2004; 140 (2)
Intrathoracic Kidney in a Newborn with Breathing Difficulty Syndrome Secondary to Congenital Diaphragmatic Hernia.
Urdaneta-Carruyo E, Méndez-Parra A, Palencia-Molina MA, Urdaneta-Contreras A, Urdaneta-Morales A
Language: Spanish
References: 24
Page: 219-224
PDF size: 1055.10 Kb.
ABSTRACT
Congenital diaphragmatic hernia (CDH) is found frequently
in from 0.17 to 0.57 among 1000 newborns and is associated
with intrathoracic kidney (IK) in 0.25%. The objective of the
present work was to describe both present pathologies in a
newborn and to review the literature in this respect.
Clinical case: male newborns, who presented tachypnea
sudden and persistent for the first 24 h of life. For the that
was physical exam, we included breathing difficulty (eight
points of Silverman’s) and cyanosis; initial arterial gases:
hypoxemia and hypocapnia (acute respiratory failure type
I); thorax X-ray; increase of bronchial plot and of parahiliary
density; normal lungs, pleuro-peritoneal membrane and solid
mass superimposed on heart silhouette were observed and
confirmed by echocardiogram. Computed axial tomography
(CAT) revealed left kidney and part of spleen inside thorax,
beside inferior lobe of left lung. Immediately, the patient was
mechanically ventilated and after 2 days, was operated
sourgically for correction of CDH and descent of left kidney.
After surgical intervention, initial syntomatology disappeared
and evolution was satisfactory. The present case illustrates
how the kidney on occasion can emigrate due to congenital
default to the thorax of the wall of the diaphragm and be a
casual discovery at the moment of radiologic exploration.
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