Author/Authors :
پاندي، شانتانو نويسنده Department of Nuclear Medicine & PET/CT, Amrita Institute of Medical Sciences, Cochin, Kerala, India Pande, Shantanu , پادما، سابرامانيام نويسنده Department of Nuclear Medicine & PET/CT, Amrita Institute of Medical Sciences, Cochin, Kerala, India Padma, Subramanyam , شانموگا سوندرام، پالانيسوامي نويسنده Department of Nuclear Medicine & PET/CT, Amrita Institute of Medical Sciences, Cochin, Kerala, India Sundaram, Palaniswamy
Abstract :
Congenital diaphragmatic hernia (CDH) is a rare anomaly with a reported incidence of 1 in 16,000 populations. It may be
associated with herniation of stomach, intestinal loops, spleen, and kidney through a chest wall defect. We report a case of a
1 year old male child who presented with recurrent fever, occasional chills and rigor of 4 months duration. Left kidney was
non visualised on ultrasound examination. Patient was referred for a 99mTc DTPA (Diethylenetriamine penta-acetic acid)
renogram to look for the presence of an ectopic left kidney. An intrathoracic left kidney was identified that was normally
functioning and PUJ (pelviureteric junction) non obstructed. A routine chest X-ray was performed to look for respiratory
tract infection that showed bowel loops in left posterior thorax, raising a suspicion for CDH. The patient underwent
thoracoscopic repair of CDH and the hernial contents were found to be left kidney, intestinal loops and spleen. Intrathoracic
kidney is relatively rare and constitutes 5% of all ectopic kidneys and is invariably PUJ non obstructed.