Clear cell renal cell carcinoma

The Clear Cell Renal Cell Carcinoma (CCRCC) is a type of renal cell carcinoma.

Genetics[]

Cytogenetics[]

• Alterations of chromosome 3p segments occurs in 70 – 90% of CCRCCs
• Inactivation of von Hippel-Lindau disease (VHL) gene by gene mutation and
• Gain of chromosome 5q
• Loss of chromosomes 8p, 9p, and 14q

Molecular genetics[]

Several frequently mutated genes were discovered in CCRCC: VHL, KDM6A/UTX, SETD2, KDM5C/JARID1C and MLL2. PBRM1 is also commonly mutated in CCRCC.^{[citation needed]}

Histogenesis[]

CCRCC is derived from the proximal convoluted tubule.^{[citation needed]}

Microscopy[]

Generally, the cells have a clear cytoplasm, are surrounded by a distinct cell membrane and contain round and uniform nuclei.^{[citation needed]}

Microscopically, CCRCCs are graded by the ISUP/WHO as follows:^[1][2]

• Grade 1: Inconspicuous and basophilic nucleoli at ×400 magnification
• Grade 2: Clearly visible and eosinophilic nucleoli at ×400 magnification
• Grade 3: Clearly visible nucleoli at ×100 magnification
• Grade 4: Extreme pleomorphism or rhabdoid and/or sarcomatoid morphology

Epidemiology[]

• Most commonly affects male patients in their sixties and seventies.
• Majority of CCRCC arise sporadically.
• Only 2 – 4% of the cases presenting as part of an inherited cancer syndrome, such as von Hippel-Lindau syndrome.

Images[]

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  Clear cell renal cell carcinoma. Macroscopy.

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  Clear cell renal cell carcinoma. HE, x100.

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  Clear cell renal cell carcinoma. Führman Grade = 1. HE, x400.

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  Grade 3: Arrows point at a clearly visible nucleolus

References[]