Korean J Urol. 2006 Dec;47(12):1367-1370. Korean.
Published online Dec 31, 2006.
Copyright © 2006 The Korean Urological Association
Case Report

Xanthogranulomatous Pyelonephritis in an Infant

Ha Na Lee, Kyu Hyun Kim, In Wook Ryu, Min Cheol Han and Woo Sik Chung
    • Department of Urology, Ewha Womans University College of Medicine, Seoul, Korea.
Received July 18, 2006; Accepted August 09, 2006.

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.

Keywords
Xanthogranulomatous pyelonephritis; Infant

Figures

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).

References

    1. Hammadeh MY, Nicholls G, Calder CJ, Buick RG, Gornall P, Corkery JJ. Xanthogranulomatous pyelonephritis in childhood: pre-operative diagnosis is possible. Br J Urol 1994;73:83–86.
    1. Samuel M, Duffy P, Capps S, Mouriquand P, Williams D, Ransley P. Xanthogranulomatous pyelonephritis in childhood. J Pediatr Surg 2001;36:598–601.
    1. Jeong KS, Kim DS, Cho JH. A cases of xanthogranulomatous pyelonephritis in children. Korean J Urol 1994;35:82–85.
    1. Avnet NL, Roberts TW, Goldberg HR. Temefactive xanthogranulomatous pyelonephritis. Am J Roentgenol Radium Ther Nucl Med 1963;90:80–96.
    1. Choi SH, Lee JH, Cho SR. Xanthogranulomatous pyelonephritis in a child. Korean J Urol 2005;46:1231–1234.
    1. Kural AR, Akaydin A, Oner A, Ozbay G, Solok V, Oruc N, et al. Xanthogranulomatous pyelonephritis in children and adults. Br J Urol 1987;59:383–385.
    1. Kang TW, Jung SI, Jung GW. Clinical studies of xanthogranulomatous pyelonephritis. Korean J Urol 2001;42:279–284.
    1. Dunnick NR, Sandler CM, Amis ES, Newhouse JH. Renal inflammatory disease. In: Dunnick NR, Sandler CM, Amis ES, Newhouse JH, editors. Textbook of uroradiology. 2nd ed. Baltimore: Williams & Wilkins; 1997. pp. 163-189.
    1. Rasoulpour M, Banco L, Mackay IM, Height DW, Berman MM. Treatment of focal xanthogranulomatous pyelonephritis with antibiotics. J Pediatr 1984;105:423–425.
    1. Sugie S, Tanaka T, Nishikawa A, Yoshimi N, Kato K, Mori H, et al. Fine-needle aspiration cytology of xanthogranulomatous pyelonephritis. Urology 1991;37:376–379.

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