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Case Report

Congenital Megacalycosis with IgA Nephropathy: A Case Report and Review of the Literature

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Pages 155-158 | Received 07 Jun 2012, Accepted 09 Sep 2012, Published online: 20 Dec 2012

Figures & data

Figure 1.  Magnetic resonance urography revealed calyceal dilatation, increased number of calyces, and normal ureters and bladder.

Figure 1.  Magnetic resonance urography revealed calyceal dilatation, increased number of calyces, and normal ureters and bladder.

Figure 2.  Glomeruli had no significant alterations light microscopically [(A) hematoxylin and eosin stain, ×200 magnification and (B) Masson’s trichrome stain, ×400 magnification].

Figure 2.  Glomeruli had no significant alterations light microscopically [(A) hematoxylin and eosin stain, ×200 magnification and (B) Masson’s trichrome stain, ×400 magnification].

Figure 3.  Mild tubular atrophy with interstitial fibrosis is noted at right side of the picture (Jone’s methanamine silver stain, × 200 magnification). Inset shows deposition of IgA in the mesangial regions (imunofluorescence, fluorescein isothiocyanate-conjugated anti-IgA antibody ×400).

Figure 3.  Mild tubular atrophy with interstitial fibrosis is noted at right side of the picture (Jone’s methanamine silver stain, × 200 magnification). Inset shows deposition of IgA in the mesangial regions (imunofluorescence, fluorescein isothiocyanate-conjugated anti-IgA antibody ×400).

Table 1.  Clinical and demographic characteristics of the cases with congenital megacalycosis described in the literature.

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