Tumores renales. Entidades frecuentes y nuevos conceptos (OMS, 2016)

Moch H, Humphrey PA, Ulbright TM, Reuter VE. WHO Classification of Tumours of the Urinary System and Male Genital Organs. World Health Organization: International Agency for Research on Cancer, Lyon, France; 2016. Eble JN, Sauter G, Epstein J, Sesterhen I. Pathology and Genetics of Tumours of the Urinary System and Male Genital Organs. World Health Organization: International Agency for Research on Cancer, Lyon, France; 2004. Srigley, 2013, The International Society of Urological Pathology (ISUP) Vancouver Classification of Renal Neoplasia, Am J Surg Pathol, 37, 1469, 10.1097/PAS.0b013e318299f2d1 Perrino, 2018, Morphological spectrum of renal cell carcinoma, unclassified: an analysis of 136 cases, Histopathology, 72, 305, 10.1111/his.13362 Kuroda, 2015, Sporadic renal hemangioblastoma with CA9, PAX2 and PAX8 expression: diagnostic pitfall in the differential diagnosis from clear cell renal cell carcinoma, Int J Clin Exp Pathol, 8, 2131 Gupta, 2015, Diagnostic approach to hereditary renal cell carcinoma, AJR Am J Roentgenol, 204, 1031, 10.2214/AJR.14.13514 Pal, 2018, Characterization of clinical cases of advanced papillary renal cell carcinoma via comprehensive genomic profiling, Eur Urol, 73, 71, 10.1016/j.eururo.2017.05.033 Cancer Genome Atlas Research Network, 2016, Comprehensive molecular characterization of papillary renal-cell carcinoma, N Engl J Med, 374, 135, 10.1056/NEJMoa1505917 Daugherty, 2016, Chromophobe renal cell carcinoma is the most common nonclear renal cell carcinoma in young women: results from the SEER Database, J Urol, 195, 847, 10.1016/j.juro.2015.10.177 Hasumi, 2016, Birt-Hogg-Dubé syndrome: clinical and molecular aspects of recently identified kidney cancer syndrome, Int J Urol, 23, 204, 10.1111/iju.13015 Delahunt, 2007, Fuhrman grading is not appropriate for chromophobe renal cell carcinoma, Am J Surg Pathol, 31, 957, 10.1097/01.pas.0000249446.28713.53 Thway, 2012, Metastatic renal mucinous tubular and spindle cell carcinoma. Atypical behavior of a rare, morphologically bland tumor, Ann Diagn Pathol, 16, 407, 10.1016/j.anndiagpath.2011.04.001 Schieda, 2015, Ten uncommon and unusual variants of renal angiomyolipoma (AML): radiologic-pathologic correlation, Clin Radiol, 70, 206, 10.1016/j.crad.2014.10.001 Brimo, 2010, Renal epithelioid angiomyolipoma with atypia: a series of 40 cases with emphasis on clinicopathologic prognostic indicators of malignancy, Am J Surg Pathol, 34, 715, 10.1097/PAS.0b013e3181d90370 Guo, 2016, Malignant renal epithelioid angiomyolipoma: a case report and review of the literature, Oncol Lett, 11, 95, 10.3892/ol.2015.3846 Trpkov, 2010, Renal oncocytoma revisited: a clinicopathological study of 109 cases with emphasis on problematic diagnostic features, Histopathology, 57, 893, 10.1111/j.1365-2559.2010.03726.x Hes, 2008, Renal oncocytoma with and without intravascular extension into the branches of renal vein have the same morphological, immunohistochemical and genetic features, Virchows Arch, 452, 285, 10.1007/s00428-007-0564-7 Carter, 2017, Immunohistochemical characterization of fumarate hydratase (FH) and succinate dehydrogenase (SDH) in cutaneous leiomyomas for detection of familial cancer syndromes, Am J Surg Pathol, 41, 801, 10.1097/PAS.0000000000000840 Vocke, 2017, Comprehensive genomic and phenotypic characterization of germline FH deletion in hereditary leiomyomatosis and renal cell carcinoma, Genes Chromosomes Cancer, 56, 484, 10.1002/gcc.22452 Gill, 2011, Renal tumors and hereditary pheochromocytoma-paraganglioma syndrome type 4, N Engl J Med, 364, 885, 10.1056/NEJMc1012357 Gill, 2014, Succinate dehydrogenase (SDH)-deficient renal carcinoma: a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients, Am J Surg Pathol, 38, 1588, 10.1097/PAS.0000000000000292 Smith, 2016, Tubulocystic carcinoma of the kidney with poorly differentiated foci: a frequent morphologic pattern of fumarate hydratase-deficient renal cell carcinoma, Am J Surg Pathol, 40, 1457, 10.1097/PAS.0000000000000719 Tickoo, 2006, Spectrum of epithelial neoplasms in end-stage renal disease: an experience from 66 tumor-bearing kidneys with emphasis on histologic patterns distinct from those in sporadic adult renal neoplasia, Am J Surg Pathol, 30, 141, 10.1097/01.pas.0000185382.80844.b1 Foshat, 2017, Acquired cystic disease-associated renal cell carcinoma: review of pathogenesis, morphology, ancillary tests, and clinical features, Arch Pathol Lab Med, 141, 600, 10.5858/arpa.2016-0123-RS Shao, 2016, Clear cell papillary renal cell carcinoma as part of histologically discordant multifocal renal cell carcinoma: a case report and review of literature, Pathol Res Pract, 212, 229, 10.1016/j.prp.2015.12.007 Aron, 2015, Am J Surg Pathol, 39, 873, 10.1097/PAS.0000000000000446 Camparo, 2008, Renal translocation carcinomas: clinicopathologic, immunohistochemical, and gene expression profiling analysis of 31 cases with a review of the literature, Am J Surg Pathol, 32, 656, 10.1097/PAS.0b013e3181609914 Sirohi, 2017, Renal cell carcinoma, unclassified with medullary phenotype: poorly differentiated adenocarcinomas overlapping with renal medullary carcinoma, Hum Pathol, 67, 134, 10.1016/j.humpath.2017.07.006 Amin, 2014, Collecting duct carcinoma versus renal medullary carcinoma: an appeal for nosologic and biological clarity, Am J Surg Pathol, 38, 871, 10.1097/PAS.0000000000000222 Montironi, 2008, Cystic nephroma and mixed epithelial and stromal tumour of the kidney: opposite ends of the spectrum of the same entity?, Eur Urol, 54, 1237, 10.1016/j.eururo.2007.10.040 Schultz, 2017, PTEN, DICER1, FH, and their associated tumor susceptibility syndromes: clinical features, genetics, and surveillance recommendations in childhood, Clin Cancer Res, 23, e76, 10.1158/1078-0432.CCR-17-0629