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Chromophobe Renal Cell Carcinoma With Extensive Retraction Artifact: A Potential Diagnostic Pitfall From Micropapillary Urothelial Carcinoma
AR. Sangoi, K. Pivovarcikova, M. Akgul, SR. Williamson, M. Ulamec, JD. Rogala, P. Martinek, T. Vanecek, O. Hes, R. Alaghehbandan
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
- MeSH
- artefakty * MeSH
- diferenciální diagnóza MeSH
- karcinom z přechodných buněk diagnóza patologie chirurgie MeSH
- karcinom z renálních buněk * diagnóza patologie chirurgie genetika MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádorové biomarkery analýza genetika MeSH
- nádory ledvin * patologie diagnóza chirurgie genetika MeSH
- papilární karcinom patologie diagnóza chirurgie MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
In addition to "classic" and eosinophilic subtype, chromophobe renal cell carcinoma (RCC) is well-known to demonstrate various morphological patterns including adenomatoid, microcystic, pigmented, multicystic, papillary, neuroendocrine-like, and small cell-like, all of which are important to appreciate for accurate diagnosis. Herein, we expand on a unique chromophobe RCC morphology not previously described consisting of tumor cells with extensive stromal retraction, mimicking upper urothelial tract micropapillary carcinoma (MPC). Twelve MPC-like chromophobe RCC nephrectomies were reviewed with clinicopathological features recorded; molecular testing was performed on 7 of 12 tumors. Patients were mostly men (n=10) with a mean age of 65 years. Mean tumor size was 6.4 cm with pathological stage distribution as follows: 4 (33%) T1a, 2 (17%) T1b, 1 (8%) T2b, and 3 (25%) T3a. The extent of MPC-like chromophobe RCC foci ranged from 10% to 40% (mean=26%; there was no correlation between the extent of MPC-like chromophobe RCC foci and tumor stage). Other chromophobe RCC morphological patterns were not identified. When performed, all (100%) tumors depicted prototypic chromophobe RCC staining pattern of KIT positivity/KRT7 positivity. Molecular showed 6 of 7 (86%) with multiple chromosomal losses. Clinically significant mutations were identified in NF1, TP53, FLCN (likely somatic), CHEK2, and ZFHX3 genes. Follow up available in 9 patients showed no evidence of disease (mean=23 months). Although the etiology behind the extensive stromal retraction in our tumors is unknown, this may likely be artifactual in nature. Nonetheless, it is important to include MPC-like chromophobe RCC in the spectrum of "variant" morphologies to avoid diagnostic pitfalls from micropapillary carcinoma.
Department of Pathology and Laboratory Medicine Albany Medical Center Albany NY USA
Department of Pathology Charles University Hospital and Medical Facility Plzen Plzen Czech Republic
Department of Pathology Public Specialist Hospital Nowa Sól Poland
Department of Pathology Regional Specialist Hospital Wrocław
Department of Pathology Stanford Medical Center Stanford CA USA
Citace poskytuje Crossref.org
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