Acceptance of emerging renal oncocytic neoplasms: a survey of urologic pathologists

. 2024 Nov ; 485 (5) : 829-840. [epub] 20240917

Jazyk angličtina Země Německo Médium print-electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid39287823

Grantová podpora
P30 CA008748 NCI NIH HHS - United States

Odkazy

PubMed 39287823
PubMed Central PMC11564393
DOI 10.1007/s00428-024-03909-2
PII: 10.1007/s00428-024-03909-2
Knihovny.cz E-zdroje

Oncocytic renal neoplasms are a major source of diagnostic challenge in genitourinary pathology; however, they are typically nonaggressive in general, raising the question of whether distinguishing different subtypes, including emerging entities, is necessary. Emerging entities recently described include eosinophilic solid and cystic renal cell carcinoma (ESC RCC), low-grade oncocytic tumor (LOT), eosinophilic vacuolated tumor (EVT), and papillary renal neoplasm with reverse polarity (PRNRP). A survey was shared among 65 urologic pathologists using SurveyMonkey.com (Survey Monkey, Santa Clara, CA, USA). De-identified and anonymized respondent data were analyzed. Sixty-three participants completed the survey and contributed to the study. Participants were from Asia (n = 21; 35%), North America (n = 31; 52%), Europe (n = 6; 10%), and Australia (n = 2; 3%). Half encounter oncocytic renal neoplasms that are difficult to classify monthly or more frequently. Most (70%) indicated that there is enough evidence to consider ESC RCC as a distinct entity now, whereas there was less certainty for LOT (27%), EVT (29%), and PRNRP (37%). However, when combining the responses for sufficient evidence currently and likely in the future, LOT and EVT yielded > 70% and > 60% for PRNRP. Most (60%) would not render an outright diagnosis of oncocytoma on needle core biopsy. There was a dichotomy in the routine use of immunohistochemistry (IHC) in the evaluation of oncocytoma (yes = 52%; no = 48%). The most utilized IHC markers included keratin 7 and 20, KIT, AMACR, PAX8, CA9, melan A, succinate dehydrogenase (SDH)B, and fumarate hydratase (FH). Genetic techniques used included TSC1/TSC2/MTOR (67%) or TFE3 (74%) genes and pathways; however, the majority reported using these very rarely. Only 40% have encountered low-grade oncocytic renal neoplasms that are deficient for FH. Increasing experience with the spectrum of oncocytic renal neoplasms will likely yield further insights into the most appropriate work-up, classification, and clinical management for these entities.

Department of Pathology Advanced Medical Research Institute Hospital Kolkata India

Department of Pathology Albany Medical Centre Albany USA

Department of Pathology All India Institute of Medical Sciences Bhubaneswar India

Department of Pathology All India Institute of Medical Sciences New Delhi India

Department of Pathology Apollo Hospitals Bhubaneshwar Bhubaneswar India

Department of Pathology Basavatakaram Indo American Cancer Hospital and Research Institute Hyderabad India

Department of Pathology Bioptika Laborator S R O Pilsen Czech Republic

Department of Pathology Brigham and Women's Hospital Boston USA

Department of Pathology Brown University Providence USA

Department of Pathology Cedars Sinai Medical Center Los Angeles USA

Department of Pathology Cleveland Clinic Cleveland USA

Department of Pathology Core Diagnostics Gurgaon India

Department of Pathology Cruces University Hospital Barakaldo Spain

Department of Pathology Douglass Hanly Moir Pathology Sydney Australia

Department of Pathology El Camino Hospital Mountain View USA

Department of Pathology Henry Ford Health System Detroit USA

Department of Pathology Homi Bhabha Cancer Center Visakhapatnam India

Department of Pathology Kapoor Center of Urology and Pathology Raipur India

Department of Pathology Keck School of Medicine of USC Los Angeles USA

Department of Pathology Kochi Red Cross Hospital Kochi City Kochi Japan

Department of Pathology Kokilaben Ambani Hospital Mumbai India

Department of Pathology Loyola University Medical Center Maywood USA

Department of Pathology Memorial Sloan Kettering Cancer Center New York USA

Department of Pathology Muljibhai Patel Urological Hospital Nadiad India

Department of Pathology Ohio State University Columbus USA

Department of Pathology Oxford University Hospital NHS Foundation Trust Oxford UK

Department of Pathology Postgraduate Institute of Medical Education and Research Chandigarh India

Department of Pathology Tata Medical Center Kolkata India

Department of Pathology Tata Memorial Hospital Mumbai India

Department of Pathology The University of North Carolina at Chapel Hill Chapel Hill USA

Department of Pathology The University of Tennessee Health Science Center Memphis USA

Department of Pathology The University of Texas MD Anderson Cancer Center Houston USA

Department of Pathology Trillium Health Partners Credit Valley Hospital Mississauga Canada

Department of Pathology Tufts University School of Medicine Boston USA

Department of Pathology University Hospital Zurich Switzerland

Department of Pathology University of Calgary Calgary Canada

Department of Pathology University of Chicago Chicago USA

Department of Pathology University of Michigan Ann Arbor USA

Department of Pathology University of Turin Turin Italy

Department of Pathology University of Utah ARUP Salt Lake City USA

Department of Pathology University of Verona Verona Italy

Department of Pathology University of Washington Seattle USA

Department of Pathology UT Southwestern Medical Center Dallas USA

Department of Pathology Vanderbilt University Medical Center Nashville USA

Department of Pathology Virginia Commonwealth University School of Medicine Richmond USA

Department of Pathology Wellington School Medicine Wellington New Zealand

IMP Pathology Garden City USA

Zobrazit více v PubMed

Hes O, Trpkov K (2022) Do we need an updated classification of oncocytic renal tumors? : emergence of low-grade oncocytic tumor (LOT) and eosinophilic vacuolated tumor (EVT) as novel renal entities. Mod Pathol 35(9):1140–1150 PubMed

Amin MB, McKenney JK, Martignoni G, Campbell SC, Pal S, Tickoo SK (2022) Low grade oncocytic tumors of the kidney: a clinically relevant approach for the workup and accurate diagnosis. Mod Pathol 35(10):1306–1316 PubMed

Samaratunga H, Egevad L, Thunders M, Iczskowski KA, van der Kwast T, Kristiansen G et al (2022) LOT and HOT … or not. The proliferation of clinically insignificant and poorly characterised types of renal neoplasia. Pathology 54(7):842–7 PubMed

Siadat F, Trpkov K (2020) ESC, ALK, HOT and LOT: three letter acronyms of emerging renal entities knocking on the door of the WHO classification. Cancers (Basel) 12(1):168 PubMed PMC

Trpkov K, Williamson SR, Gill AJ, Adeniran AJ, Agaimy A, Alaghehbandan R et al (2021) Novel, emerging and provisional renal entities: the Genitourinary Pathology Society (GUPS) update on renal neoplasia. Mod Pathol 34(6):1167–1184 PubMed

Argani P, McKenney JK, Hartmann A, Hes O, Magi-Galluzzi C, Trpkov K (2022) Eosinophilic solid and cystic renal cell carcinoma: IARC [Available from: https://tumourclassification.iarc.who.int/chaptercontent/36/23 PubMed

McKenney JK, Przybycin CG, Trpkov K, Magi-Galluzzi C (2018) Eosinophilic solid and cystic renal cell carcinomas have metastatic potential. Histopathology 72(6):1066–1067 PubMed

Mehra R, Vats P, Cao X, Su F, Lee ND, Lonigro R et al (2018) Somatic Bi-allelic loss of TSC genes in eosinophilic solid and cystic renal cell carcinoma. Eur Urol 74(4):483–486 PubMed PMC

Palsgrove DN, Li Y, Pratilas CA, Lin MT, Pallavajjalla A, Gocke C et al (2018) Eosinophilic solid and cystic (ESC) renal cell carcinomas harbor TSC mutations: molecular analysis supports an expanding clinicopathologic spectrum. Am J Surg Pathol 42(9):1166–1181 PubMed PMC

Parilla M, Kadri S, Patil SA, Ritterhouse L, Segal J, Henriksen KJ et al (2018) Are sporadic eosinophilic solid and cystic renal cell carcinomas characterized by somatic tuberous sclerosis gene mutations? Am J Surg Pathol 42(7):911–917 PubMed

Trpkov K, Abou-Ouf H, Hes O, Lopez JI, Nesi G, Comperat E et al (2017) Eosinophilic solid and cystic renal cell carcinoma (ESC RCC): further morphologic and molecular characterization of ESC RCC as a distinct entity. Am J Surg Pathol 41(10):1299–1308 PubMed

Trpkov K, Hes O, Bonert M, Lopez JI, Bonsib SM, Nesi G et al (2016) Eosinophilic, solid, and cystic renal cell carcinoma: clinicopathologic study of 16 unique, sporadic neoplasms occurring in women. Am J Surg Pathol 40(1):60–71 PubMed

Williamson SR, Gadde R, Trpkov K, Hirsch MS, Srigley JR, Reuter VE et al (2017) Diagnostic criteria for oncocytic renal neoplasms: a survey of urologic pathologists. Hum Pathol 63:149–156 PubMed

Akgul M, Al-Obaidy KI, Cheng L, Idrees MT (2021) Low-grade oncocytic tumour expands the spectrum of renal oncocytic tumours and deserves separate classification: a review of 23 cases from a single tertiary institute. J Clin Pathol 75:772 PubMed

Guo Q, Liu N, Wang F, Guo Y, Yang B, Cao Z et al (2021) Characterization of a distinct low-grade oncocytic renal tumor (CD117-negative and cytokeratin 7-positive) based on a tertiary oncology center experience: the new evidence from China. Virchows Arch 478(3):449–458 PubMed

Kapur P, Gao M, Zhong H, Chintalapati S, Mitui M, Barnes SD et al (2021) Germline and sporadic mTOR pathway mutations in low-grade oncocytic tumor of the kidney. Mod Pathol 35:333–343 PubMed PMC

Kravtsov O, Gupta S, Cheville JC, Sukov WR, Rowsey R, Herrera-Hernandez LP et al (2021) Low-grade oncocytic tumor of kidney (CK7-positive, CD117-negative): incidence in a single institutional experience with clinicopathological and molecular characteristics. Hum Pathol 114:9–18 PubMed

Morini A, Drossart T, Timsit MO, Sibony M, Vasiliu V, Gimenez-Roqueplo AP et al (2021) Low-grade oncocytic renal tumor (LOT): mutations in mTOR pathway genes and low expression of FOXI1. Mod Pathol 35:352–360 PubMed

Trpkov K, Williamson SR, Gao Y, Martinek P, Cheng L, Sangoi AR et al (2019) Low-grade oncocytic tumour of kidney (CD117-negative, cytokeratin 7-positive): a distinct entity? Histopathology 75(2):174–184 PubMed

Williamson SR, Hes O, Trpkov K, Aggarwal A, Satapathy A, Mishra S et al (2023) Low-grade oncocytic tumour of the kidney is characterised by genetic alterations of TSC1, TSC2, MTOR or PIK3CA and consistent GATA3 positivity. Histopathology 82(2):296–304 PubMed

Alghamdi M, Chen JF, Jungbluth A, Koutzaki S, Palmer MB, Al-Ahmadie HA et al (2024) L1 cell adhesion molecule (L1CAM) expression and molecular alterations distinguish low-grade oncocytic tumor from eosinophilic chromophobe renal cell carcinoma. Mod Pathol 37(5):100467 PubMed PMC

Chen YB, Mirsadraei L, Jayakumaran G, Al-Ahmadie HA, Fine SW, Gopalan A et al (2019) Somatic mutations of TSC2 or MTOR characterize a morphologically distinct subset of sporadic renal cell carcinoma with eosinophilic and vacuolated cytoplasm. Am J Surg Pathol 43(1):121–131 PubMed PMC

Farcas M, Gatalica Z, Trpkov K, Swensen J, Zhou M, Alaghehbandan R et al (2021) Eosinophilic vacuolated tumor (EVT) of kidney demonstrates sporadic TSC/MTOR mutations: next-generation sequencing multi-institutional study of 19 cases. Mod Pathol 34:2243 PubMed

He H, Trpkov K, Martinek P, Isikci OT, Maggi-Galuzzi C, Alaghehbandan R et al (2018) “High-grade oncocytic renal tumor”: morphologic, immunohistochemical, and molecular genetic study of 14 cases. Virchows Arch 473(6):725–738 PubMed

Tjota M, Chen H, Parilla M, Wanjari P, Segal J, Antic T (2020) Eosinophilic renal cell tumors with a TSC and MTOR gene mutations are morphologically and immunohistochemically heterogenous: clinicopathologic and molecular study. Am J Surg Pathol 44:943–954 PubMed

Trpkov K, Bonert M, Gao Y, Kapoor A, He H, Yilmaz A et al (2019) High-grade oncocytic tumour (HOT) of kidney in a patient with tuberous sclerosis complex. Histopathology 75(3):440–442 PubMed

Salles DC, Asrani K, Woo J, Vidotto T, Liu HB, Vidal I et al (2022) GPNMB expression identifies TSC1/2/mTOR-associated and MiT family translocation-driven renal neoplasms. J Pathol 257:158–171 PubMed PMC

Li H, Argani P, Halper-Stromberg E, Lotan TL, Merino MJ, Reuter VE et al (2023) Positive GPNMB immunostaining differentiates renal cell carcinoma with fibromyomatous stroma associated with TSC1/2/MTOR alterations from others. Am J Surg Pathol 47(11):1267–1273 PubMed PMC

Richard PO, Jewett MA, Bhatt JR, Evans AJ, Timilsina N, Finelli A (2016) Active surveillance for renal neoplasms with oncocytic features is safe. J Urol 195(3):581–586 PubMed

Guo J, Tretiakova MS, Troxell ML, Osunkoya AO, Fadare O, Sangoi AR et al (2014) Tuberous sclerosis-associated renal cell carcinoma: a clinicopathologic study of 57 separate carcinomas in 18 patients. Am J Surg Pathol 38(11):1457–1467 PubMed

Yang P, Cornejo KM, Sadow PM, Cheng L, Wang M, Xiao Y et al (2014) Renal cell carcinoma in tuberous sclerosis complex. Am J Surg Pathol 38(7):895–909 PubMed PMC

Kunju LP, Wojno K, Wolf JS Jr, Cheng L, Shah RB (2008) Papillary renal cell carcinoma with oncocytic cells and nonoverlapping low grade nuclei: expanding the morphologic spectrum with emphasis on clinicopathologic, immunohistochemical and molecular features. Hum Pathol 39(1):96–101 PubMed

Al-Obaidy KI, Eble JN, Cheng L, Williamson SR, Sakr WA, Gupta N et al (2019) Papillary renal neoplasm with reverse polarity: a morphologic, immunohistochemical, and molecular study. Am J Surg Pathol 43(8):1099–1111 PubMed

Han G, Yu W, Chu J, Liu Y, Jiang Y, Li Y et al (2017) Oncocytic papillary renal cell carcinoma: a clinicopathological and genetic analysis and indolent clinical course in 14 cases. Pathol Res Pract 213(1):1–6 PubMed

Lefevre M, Couturier J, Sibony M, Bazille C, Boyer K, Callard P et al (2005) Adult papillary renal tumor with oncocytic cells: clinicopathologic, immunohistochemical, and cytogenetic features of 10 cases. Am J Surg Pathol 29(12):1576–1581 PubMed

Nemours S, Armesto M, Arestin M, Manini C, Giustetto D, Sperga M et al (2024) Non-coding RNA and gene expression analyses of papillary renal neoplasm with reverse polarity (PRNRP) reveal distinct pathological mechanisms from other renal neoplasms. Pathology 56(4):493–503 PubMed

Kiyozawa D, Iwasaki T, Takamatsu D, Kohashi K, Miyamoto T, Fukuchi G et al (2024) Papillary renal neoplasm with reverse polarity has low frequency of alterations in chromosomes 7, 17, and Y. Virchows Arch 485:299–306 PubMed

Castillo VF, Trpkov K, Van der Kwast T, Rotondo F, Hamdani M, Saleeb R (2024) Papillary renal neoplasm with reverse polarity is biologically and clinically distinct from eosinophilic papillary renal cell carcinoma. Pathol Int 74(4):222–226 PubMed PMC

Satturwar S, Parwani AV (2023) Cytomorphology of papillary renal neoplasm with reverse polarity. Cytojournal 20:43 PubMed PMC

Nova-Camacho LM, Martin-Arruti M, Diaz IR, Panizo-Santos A (2023) Papillary renal neoplasm with reverse polarity: a clinical, pathologic, and molecular study of 8 renal tumors from a single institution. Arch Pathol Lab Med 147(6):692–700 PubMed

Kim B, Lee S, Moon KC (2023) Papillary renal neoplasm with reverse polarity: a clinicopathologic study of 43 cases with a focus on the expression of KRAS signaling pathway downstream effectors. Hum Pathol 142:1–6 PubMed

Yang T, Kang E, Zhang L, Zhuang J, Li Y, Jiang Y et al (2022) Papillary renal neoplasm with reverse polarity may be a novel renal cell tumor entity with low malignant potential. Diagn Pathol 17(1):66 PubMed PMC

Wei S, Kutikov A, Patchefsky AS, Flieder DB, Talarchek JN, Al-Saleem T et al (2022) Papillary renal neoplasm with reverse polarity is often cystic: report of 7 cases and review of 93 cases in the literature. Am J Surg Pathol 46(3):336–343 PubMed

Wang T, Ding X, Huang X, Ye J, Li H, Cao S et al (2022) Papillary renal neoplasm with reverse polarity-a comparative study with CCPRCC, OPRCC, and PRCC1. Hum Pathol 129:60–70 PubMed

Shen M, Yin X, Bai Y, Zhang H, Ru G, He X et al (2022) Papillary renal neoplasm with reverse polarity: a clinicopathological and molecular genetic characterization of 16 cases with expanding the morphologic spectrum and further support for a novel entity. Front Oncol 12:930296 PubMed PMC

Liu Y, Zhang H, Li X, Wang S, Zhang Y, Zhang X et al (2022) Papillary renal neoplasm with reverse polarity with a favorable prognosis should be separated from papillary renal cell carcinoma. Hum Pathol 127:78–85 PubMed

Conde-Ferreiros M, Dominguez-de Dios J, Juaneda-Magdalena L, Bellas-Pereira A, San Miguel Fraile MP, PeteiroCancelo MA et al (2022) Papillary renal cell neoplasm with reverse polarity: a new subtype of renal tumour with favorable prognosis. Actas Urol Esp (Engl Ed) 46(10):600–5 PubMed

Al-Obaidy KI, Saleeb RM, Trpkov K, Williamson SR, Sangoi AR, Nassiri M et al (2022) Recurrent KRAS mutations are early events in the development of papillary renal neoplasm with reverse polarity. Mod Pathol 35(9):1279–1286 PubMed

Kiyozawa D, Kohashi K, Takamatsu D, Yamamoto T, Eto M, Iwasaki T et al (2021) Morphological, immunohistochemical, and genomic analyses of papillary renal neoplasm with reverse polarity. Hum Pathol 112:48–58 PubMed

Chang HY, Hang JF, Wu CY, Lin TP, Chung HJ, Chang YH et al (2021) Clinicopathological and molecular characterisation of papillary renal neoplasm with reverse polarity and its renal papillary adenoma analogue. Histopathology 78(7):1019–1031 PubMed

Zhou L, Xu J, Wang S, Yang X, Li C, Zhou J et al (2020) Papillary renal neoplasm with reverse polarity: a clinicopathologic study of 7 cases. Int J Surg Pathol 28(7):728–734 PubMed

Kim SS, Cho YM, Kim GH, Kee KH, Kim HS, Kim KM et al (2020) Recurrent KRAS mutations identified in papillary renal neoplasm with reverse polarity-a comparative study with papillary renal cell carcinoma. Mod Pathol 33(4):690–699 PubMed

Al-Obaidy KI, Eble JN, Nassiri M, Cheng L, Eldomery MK, Williamson SR et al (2020) Recurrent KRAS mutations in papillary renal neoplasm with reverse polarity. Mod Pathol 33(6):1157–1164 PubMed

Al-Obaidy KI, Eble JN, Nassiri M, Cheng L, Eldomery MK, Williamson SR et al (2019) Recurrent KRAS mutations in papillary renal neoplasm with reverse polarity. Mod Pathol 33:1157–1164 PubMed

Pivovarcikova K, Grossmann P, Hajkova V, Alaghehbandan R, Pitra T, Perez Montiel D et al (2021) Renal cell carcinomas with tubulopapillary architecture and oncocytic cells: molecular analysis of 39 difficult tumors to classify. Ann Diagn Pathol 52:151734 PubMed

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