Renal oncocytoma: Personal experience

The Authors report their experience on kidney oncocytomas. They found 6 cases of kidney oncocytoma in 140 cases of kidney tumors. In all cases histological slides of neoplastic masses were made with traditional stains, PAS and PAS diastase and with immunohistochemical reaction for keratins (BDK) and vimentin (DAKO clone V9). They describe one of the six cases in which the diagnosis of oncocitary G3 type carcinoma was made, and another of oncocytomatosis with borderline aspects versus oncocytomal renal cell carcinoma.

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PRMT1, useful immunohistochemical marker for distinguishing renal oncocytoma and chromophobe renal cell carcinoma

10.26226/morressier.596dfd5bd462b802923881dc ◽

2017 ◽

Author(s):

Jelena Vještica

Keyword(s):

Renal Cell Carcinoma ◽

Cell Carcinoma ◽

Renal Cell ◽

Chromophobe Renal Cell Carcinoma ◽

Renal Oncocytoma ◽

Immunohistochemical Marker

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Expression of RON Proto-oncogene in Renal Oncocytoma and Chromophobe Renal Cell Carcinoma

The American Journal of Surgical Pathology ◽

10.1097/01.pas.0000128661.58697.7d ◽

2004 ◽

Vol 28 (8) ◽

pp. 1045-1050 ◽

Cited By ~ 30

Author(s):

Kurt T Patton ◽

Maria S Tretiakova ◽

Jorge L Yao ◽

Veronica Papavero ◽

Lei Huo ◽

...

Keyword(s):

Renal Cell Carcinoma ◽

Cell Carcinoma ◽

Renal Cell ◽

Chromophobe Renal Cell Carcinoma ◽

Renal Oncocytoma

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HNF1β and S100A1 are useful biomarkers for distinguishing renal oncocytoma and chromophobe renal cell carcinoma in FNA and core needle biopsies

Cancer Cytopathology ◽

10.1002/cncy.21530 ◽

2015 ◽

Vol 123 (5) ◽

pp. 298-305 ◽

Cited By ~ 16

Author(s):

James R. Conner ◽

Michelle S. Hirsch ◽

Vickie Y. Jo

Keyword(s):

Renal Cell Carcinoma ◽

Cell Carcinoma ◽

Renal Cell ◽

Chromophobe Renal Cell Carcinoma ◽

Renal Oncocytoma ◽

Core Needle

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Birt-Hogg-Dubé Syndrome: Clinicopathologic Findings and Genetic Alterations

Archives of Pathology & Laboratory Medicine ◽

10.5858/2006-130-1865-bscfag ◽

2006 ◽

Vol 130 (12) ◽

pp. 1865-1870 ◽

Cited By ~ 7

Author(s):

Brian P. Adley ◽

Norm D. Smith ◽

Ritu Nayar ◽

Ximing J. Yang

Keyword(s):

Renal Cell Carcinoma ◽

Cell Carcinoma ◽

Renal Cell ◽

English Literature ◽

Clinical Manifestations ◽

Genetic Alterations ◽

Limited Information ◽

Kidney Tumors ◽

Pulmonary Cysts ◽

Bhd Syndrome

Abstract Context.—Birt-Hogg-Dubé (BHD) syndrome is a rare clinicopathologic condition transmitted in an autosomal dominant fashion. This complex entity is characterized by cutaneous fibrofolliculomas, kidney tumors, pulmonary cysts, and spontaneous pneumothorax. Recently, the gene possibly responsible for the clinical manifestations of BHD syndrome has been cloned and characterized. The few reviews of BHD syndrome found in the English literature mostly focus on the skin lesions or genetics, with limited information on other pathologic changes, particularly the kidney lesions. Objective.—To review the literature on this subject with a special emphasis on BHD syndrome-associated renal pathology as well as recent advances in molecular genetic discovery of the BHD syndrome. Data Sources.—We used all data available after performing a literature search using MEDLINE and searching under the headings “Birt-Hogg-Dubé,” “hybrid oncocytic tumors,” and “folliculin.” Conclusions.—The presence of BHD syndrome should be investigated in any patient with multiple bilateral kidney tumors, especially if the predominant histologic type is chromophobe renal cell carcinoma or the so-called hybrid oncocytic tumor. The genetic alteration for BHD syndrome has been mapped to chromosome 17p12q11, and the gene in this region has been cloned and believed to be responsible for the BHD syndrome. The function of the BHD product, called folliculin, is still unknown, although it is speculated to be a tumor suppressor gene. Numerous mutations have been described in the BHD gene. Studies are ongoing to determine the relationship between the BHD gene and development of sporadic renal cell carcinoma and other lesions.

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Cystic renal oncocytoma and tubulocystic renal cell carcinoma: morphologic and immunohistochemical comparative study

Pathology ◽

10.1097/01.pat.0000454560.44704.b3 ◽

2014 ◽

Vol 46 ◽

pp. S135-S136

Author(s):

Faruk Skenderi ◽

Monika Ulamec ◽

Semir Vranić ◽

Nurija Bilalović ◽

Kvetoslava Peckova ◽

...

Keyword(s):

Renal Cell Carcinoma ◽

Comparative Study ◽

Cell Carcinoma ◽

Renal Cell ◽

Renal Oncocytoma

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Papillary renal cell carcinoma within a renal oncocytoma: Case report of very rare coexistence

Canadian Urological Association Journal ◽

10.5489/cuaj.1963 ◽

2014 ◽

Vol 8 (11-12) ◽

pp. 928 ◽

Cited By ~ 5

Author(s):

Cevahir Özer ◽

Mehmet Resit Gören ◽

Tulga Egilmez ◽

Nebil Bal

Keyword(s):

Renal Cell Carcinoma ◽

Case Report ◽

Cell Carcinoma ◽

Renal Cell ◽

Radical Nephrectomy ◽

Papillary Renal Cell Carcinoma ◽

Renal Oncocytoma ◽

Renal Neoplasms ◽

Renal Oncocytomas ◽

Papillary Rcc

Renal oncocytomas accounts for 3% to 9% of primary renal neoplasms. The coexistence of renal cell carcinoma (RCC) within the oncocytoma is extremely rare. We report the case of an asymptomatic 74-year-old man with papillary RCC within oncocytoma managed with left radical nephrectomy.

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