Metanephric Adenoma, Nephrogenic Rests, and Wilms' Tumor
- 1 October 2001
- journal article
- Published by Wolters Kluwer Health in The American Journal of Surgical Pathology
- Vol. 25 (10) , 1290-1296
- https://doi.org/10.1097/00000478-200110000-00010
Abstract
Metanephric adenoma (MA) is a renal tumor that is generally detected in adults and occasionally in children. These tumors usually behave in a benign fashion. Although the histogenesis of MA is unclear, a morphologic similarity to Wilms' tumor (WT) complex exists. Six cases of MA, five cases of childhood WT (CWT), two cases of adult WT (AWT), and four cases of treated MWT and/or nephrogenic rests (MWT/NR), with paraffin blocks available for use, were retrieved from the surgical pathology files of the Mayo Clinic. Clinical information was extracted from the medical record. Immunoperoxidase stains for WT1, AE1, CK7, CD57, CD56, and desmin were performed on paraffin sections from all cases. All six cases of MA were strongly and diffusely positive with antibodies to WT1 and CD57 and focally positive with antibodies to CK7. Three cases showed focal faint staining in <5% of the cells with keratin AE1. Stains for CD56 and desmin were negative. All seven cases of WT, including five CWT and two AWT, were strongly and diffusely positive with WT1 in the blastema and epithelium but showed only weak focal positivity in stromal cells. Six cases were diffusely positive for CD56 and one case showed focal positivity. Keratin AE1 was positive in one case of AWT and focally positive in the other AWT. The blastema of all cases of WT were negative for desmin, CK7, and CD57, although staining for keratin AE1, CD56, and CD57 was seen in maturing tubules of CWT cases. Of the five CWT cases, two had associated NR and two showed maturing WT after treatment. The areas of NR and maturing WT were histologically similar to MA and were composed of small tubules with uniform nuclei with no mitotic activity, scant cytoplasm, and focal calcifications. All four cases of maturing WT/NR were positive for WT1 and focally positive for CD57, CK7, and AE1. Stains for CD56 and desmin were negative except in foci of residual blastema, which stained for CD56 but lacked CD57 and CK7 staining. Five cases each of renal cell carcinoma, papillary renal cell carcinoma, and oncocytoma were negative for WT1. Two of five cases of chromophobe carcinoma showed very weak staining present in <10% of tumor nuclei. Metanephric adenoma is histogenetically related to WT and is morphologically and immunophenotypically identical to maturing WT and nephrogenic rests.Keywords
This publication has 18 references indexed in Scilit:
- Immunohistochemical Expression of WT1 by Desmoplastic Small Round Cell TumorThe American Journal of Surgical Pathology, 2000
- Simultaneous Chromosome 7 and 17 Gain and Sex Chromosome Loss Provide Evidence that Renal Metanephric Adenoma is Related to Papillary Renal Cell CarcinomaJournal of Urology, 1997
- Expression of the Wilms' tumour gene WT1 in the developing human and in paediatric renal tumours: an immunohistochemical study.Molecular Pathology, 1997
- Metaphase analysis of metanephric adenoma reveals chromosome Y loss with chromosome 7 and 17 gainUrology, 1996
- Clinicopathological Study of Fifty PatientsThe American Journal of Surgical Pathology, 1995
- A Clinicopathological, Immunohistochemical, Flow Cytometric, Cytogenetic, and Electron Microscopic Study of Seven CasesThe American Journal of Surgical Pathology, 1995
- The expression of the Wilms' tumour gene, WT1, in the developing mammalian embryoMechanisms of Development, 1993
- The candidate Wilms' tumour gene is involved in genitourinary developmentNature, 1990
- Nephrogenic Rests, Nephroblastomatosis, and the Pathogenesis of Wilms' TumorPediatric Pathology, 1990
- Anti‐Leu 7 immunoreactivity with human tumours: its value in the diagnosis of prostatic adenocarcinomaHistopathology, 1987