Metanephric adenoma: the utility of immunohistochemical and cytogenetic analyses in differential diagnosis, including solid variant papillary renal cell carcinoma and epithelial-predominant nephroblastoma
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
26248896
DOI
10.1038/modpathol.2015.81
PII: S0893-3952(22)01379-5
Knihovny.cz E-zdroje
- MeSH
- adenom diagnóza MeSH
- cytogenetické vyšetření MeSH
- diferenciální diagnóza MeSH
- dítě MeSH
- dospělí MeSH
- hybridizace in situ fluorescenční MeSH
- imunohistochemie MeSH
- karcinom z renálních buněk diagnóza MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- nádorové biomarkery analýza MeSH
- nádory ledvin diagnóza MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Wilmsův nádor diagnóza MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- nádorové biomarkery MeSH
Metanephric adenoma is a benign renal neoplasm that overlaps in morphology with the solid variant of papillary renal cell carcinoma and epithelial-predominant nephroblastoma. To aid in resolving this differential diagnosis, we investigated the utility of immunohistochemical and molecular analyses in distinguishing between these entities; the first study, to our knowledge, to use a combined approach in analyzing all three tumors. We analyzed 37 tumors originally diagnosed as metanephric adenomas (2 of which we reclassified as papillary renal cell carcinomas), 13 solid variant papillary renal cell carcinomas, and 20 epithelial-predominant nephroblastomas using a combination of immunohistochemistry and fluorescence in situ hybridization (FISH) assessing for trisomy of chromosomes 7 and 17 and loss of Y. Immunohistochemical staining was performed for CK7, AMACR, WT1, and CD57. The combination of CK7-, AMACR-, WT1+, and CD57+ was considered characteristic of metanephric adenoma. Most of the tumors originally diagnosed as metanephric adenomas (31/37) showed the expected staining pattern of metanephric adenoma (CK7-, AMACR-, WT1+, and CD57+). Of the six tumors with discordant immunophenotype, two tumors were reclassified as papillary renal cell carcinoma after cytogenetic workup. It is recommended that all adult cases histologically resembling metanephric adenoma have WT1, CD57, CK7, and AMACR immunohistochemical staining performed. If the staining pattern is characteristic for metanephric adenoma (CK7-, AMACR-, WT1+, and CD57+, including membranous staining), then no other diagnostic tests are indicated. However, if there is a different immunostaining pattern, then we recommend FISH analysis.
Department of Pathology and Laboratory Medicine Case Western Reserve University Cleveland OH USA
Department of Pathology and Laboratory Medicine Henry Ford Health System Detroit MI USA
Department of Pathology Charles University Hospital Plzeň Pilsen Czech Republic
Department of Pathology Fudan University Shanghai Cancer Center Shanghai China
Department of Pathology Groupe Hospitalier Pitié Salpêtrière Paris France
Zobrazit více v PubMed
Diagn Mol Pathol. 1996 Mar;5(1):53-64 PubMed
Mod Pathol. 1996 Mar;9(3):329-33 PubMed
Am J Surg Pathol. 1995 Jun;19(6):615-26 PubMed
Am J Surg Pathol. 1995 Oct;19(10):1101-14 PubMed
Mod Pathol. 2010 Jul;23(7):931-6 PubMed
Histopathology. 2013 May;62(6):941-53 PubMed
Mod Pathol. 2006 Feb;19(2):218-24 PubMed
Mod Pathol. 2003 Oct;16(10):1060-3 PubMed
Pathol Res Pract. 2008;204(10):719-23 PubMed
Cancer. 1995 Aug 15;76(4):669-73 PubMed
Am J Surg Pathol. 2001 Oct;25(10):1290-6 PubMed
Hum Pathol. 2009 Jan;40(1):10-29 PubMed
Clin Cancer Res. 2008 Dec 15;14(24):8087-93 PubMed
Histopathology. 2009 Apr;54(5):516-28 PubMed
Am J Surg Pathol. 2004 Sep;28(9):1117-32 PubMed
Mol Pathol. 1997 Jun;50(3):138-44 PubMed
J Pathol. 1996 Jun;179(2):162-8 PubMed
Am J Surg Pathol. 2008 Dec;32(12):1780-6 PubMed
Mod Pathol. 1997 Nov;10(11):1143-50 PubMed
Genes Chromosomes Cancer. 1991 Jul;3(4):249-55 PubMed
Clin Cancer Res. 2005 Oct 15;11(20):7226-33 PubMed
Am J Surg Pathol. 2013 Aug;37(8):1131-9 PubMed
KANK1-NTRK3 fusions define a subset of BRAF mutation negative renal metanephric adenomas
Distinct clinicopathological features in metanephric adenoma harboring BRAF mutation