My. Hammadeh et al., XANTHOGRANULOMATOUS PYELONEPHRITIS IN CHILDHOOD - PREOPERATIVE DIAGNOSIS IS POSSIBLE, British Journal of Urology, 73(1), 1994, pp. 83-86
Objective To diagnose xanthogranulomatous pyelonephritis (XGP) in chil
dhood pre-operatively. Patients and methods Eleven cases of XGP presen
ting to Birmingham Children's Hospital over a 10-year-period are repor
ted. Nine (82%) were diagnosed preoperatively on the clinical and radi
ological findings. Results The characteristic clinical findings were u
rinary tract infection (9 cases), palpable renal mass (8 cases) and an
aemia (8 cases). The most common radiological findings were enlarged k
idney (9 cases), renal calculi (7 cases) and non-functioning kidney (6
cases). Renal ultrasound typically demonstrated a central echoic area
(6 cases) and multiple hypoechoic areas in the parenchyma (7 cases).
A computed tomography (CT) scan was performed in three cases. This sho
wed characteristic multiple, low attenuation, unenhanced areas within
the parenchyma with extension of the inflammatory process into peri-ne
phric fat (two cases). Ten cases (91%) were of the diffuse type. There
was extension into the peri-nephric fat in eight cases (73%). Three c
ases (27%) were associated with congenital urological abnormalities. N
ephrectomy was performed in 10 cases and a partial nephrectomy in one.
Conclusion XGP is uncommon in childhood but should always be consider
ed in the differential diagnosis of renal masses, especially in the pr
esence of anaemia. Nephrectomy usually results in a permanent cure.