Renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions

Renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions

Definition

A group of kidney carcinomas characterized by the presence of different translocations involving the chromosome Xp11.2. These translocations result in the creation of gene fusions involving the TFE3 gene. Patients are usually children and young adults. Morphologically, the malignant epithelial cells form papillary patterns.

Also known as renal cell cancer associated with Xp11.2 translocations/TFE3 Gene fusions, renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions, TFE3-Rearranged renal cell carcinoma, tRCC, Xp11.2 translocation-related renal cell carcinoma — per MONDO

Also identified as

Affected Organs

Organ Involvement Source
Adult mammalian kidney Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Adult mammalian kidney Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Genitourinary system Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Genitourinary system Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Nephron tubule Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Renal system Disease Has Associated Anatomic Site NCIT · CC BY 4.0
Renal system Disease Has Primary Anatomic Site NCIT · CC BY 4.0
Upper urinary tract Disease Has Associated Anatomic Site NCIT · CC BY 4.0