large multicystic dysplastic kidney mimicking a large cystic renal neoplasm
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2017
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Abstract
Multicystic Dysplastic Kidney (MCDK) is one of the most common renal conditions seen in paediatric population. The natural history
typically involves involution and many of the patients with unilateral disease may actually never become symptomatic. The initial
evaluation is usually done on Ultrasonography (USG) while cross-sectional imaging and nuclear scan are reserved for diagnostic
dilemmas. Management is conservative and surgery is done for selected patients with symptomatic cysts or suspicion of neoplasm.
We present an interesting case of MCDK in a nine-month-old female hypertensive child presenting with a large abdominal mass
increasing in size with imaging features similar to cystic neoplasm and managed with nephrectomy.
| Reference Key |
yadav2017journallarge
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| Authors | ;Priyank Yadav;Sanjoy Kumar Sureka;M S Ansari;Rahul Soni;Hira Lal |
| Journal | JAMA network open |
| Year | 2017 |
| DOI |
10.7860/JCDR/2017/24226.9887
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