Unilateral Multicystic Dysplasia of the Kidneys (A Cohort of Patients)

Česká verzia

Authors: Š. Doležalová; Jakub Langer
Authors place of work: Klinika dětského a dorostového lékařství 1. LF UK a VFN, Praha přednosta prof. MUDr. J. Zeman, DrSc
Published in the journal: Čes-slov Pediat 2010; 65 (12): 676-681.
Category: Původní práce

Summary

Introduction:
„Multicystic dysplastic kidney“ (MCDK) belongs to the most frequent inherited uropathies. The objective of the article is a retrospective analysis of the disease course in 80 children with MCDK, having been under observation since 1991 to 2009.

Methods:
The authors evaluated 90 children (41 boys and 39 girls). The diagnosis of MCDK was mostly established prenatally (89%). In 13 children (17%) the dysplasia was associated with pelvic or cross dystopia of the affected kidney. DMSA was performed in 73 children (91%), Miction cystourethrography (MCUG) in 66 children (82%).

Results:
A conservative treatment was applied in 69 children (86%), nephrectomy was indicated in 11 patients (14%), mostly for extreme size of the affected kidney. In 19% of children (24%), functional or structural damage of the second kidney was confirmed (hydronephrosis 5 times, obstruction megauterus twice, vesicourethral reflux 4 times, other pathology 4 times). In most cases (96%) the unaffected kidney was demonstrated to grow within the range of compensatory hypertrophy (size above 95 percentile according to Dinkel figure). In 5 patients the renal functions decreased, always in association with the defect of the functionally solitary kidney. Laboratory signs of chronic renal insufficiency last in three patients. Hypertension was proved in five children (6%), in three of them with anomalies of the other side, two patients suffered from hypertension with normal findings on the contralateral kidney, which was mitigated after nephrectomy. Malignity of multicystic kidney was not observed in any patient. In the conservatively treated children the cystic formation completely disappeared in 28 children (41%) and in other 14 subjects (20%) there was a significant reduction of the cystic formation. The cystic kidney disappeared in 32 months on the average (1 to 141 months). In 27 cases (39%) there is a stationary finding on the affected kidney.

Conclusion:
In agreement with literature our findings document the advantages and safety of the conservative approach in children with MCDK. The probability of a significant reduction of the multicystic kidney is high in children up to three year of life, but tends to decrease with age. The prognosis of the child is significantly influenced by damage of the other kidney which should be carefully investigated.

Key words:
multicystic kidney dysplasia, DMSA scan, micturition cystourethro-graphy, vesicourethral reflux, Wilms tumor

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