Published online Dec 31, 2006.
https://doi.org/10.4111/kju.2006.47.12.1367
Xanthogranulomatous Pyelonephritis in an Infant
Abstract
Xanthogranulomatous pyelonephritis (XGP) is an uncommon, severe, chronic infection of the kidney, which results in the normal renal parenchyma being replaced by characteristic lipid-laden macrophages (foam cells). It can occur at any age, but is extremely rare in children. Herein, the case of a 6-month-3-week-old girl with XGP, pre-operatively diagnosed with a Wilms' tumor, is reported. This is the youngest age of any patient with such a condition reported in the Korean literatures. Excretory urography, abdominal sonogram, computed tomogram and magnetic resonance imaging revealed a right renal round mass, without any calcifications. Her pathological findings after a radical nephrectomy revealed XGP.
Fig. 1
Radiological findings. (A) Ultrasonography of the abdomen shows a well demarcated heterogeneous echogenic lesion with a thin echogenic rim in the middle portion of the slightly enlarged right kidney. (B) Postcontrast enhancement of abdominal computerized tomography demonstrates a well demarcated, round soft tissue density mass at the upper pole of the right kidney. (C) T1-weighted image, coronal section of a magnetic resonance image shows a heterogeneous, diffuse enhancement and irregularly shaped low signal intensity mass at the anterior aspect of the middle portion of the right kidney.
Fig. 2
Microscopic findings of the specimen reveal extensive pyelonephritis, granulomas, atrophied glomerulus and tubules, and lipid-laden macrophages (foam cells) (black arrow) and plasma cells (white arrow) (H&E, ×200).
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