Mixed epithelial and stromal tumor (MEST), including adult cystic nephroma (CN), is an uncommon benign renal neoplasm that mostly occurs in middle-aged women. To date, a comprehensive molecular genetic investigation of MEST and/or adult CN has not been performed. Fourteen archival cases of MEST were identified, and comprehensive clinicopathologic and molecular characterization was performed. Tumors arose only in female patients (median: 49 y, range: 35 to 82 y) and showed variable admixtures of bland epithelial glands, tubules, and cysts within an ovarian-type spindle cell stroma. In total, copy number alterations (CNAs) were detected in 6/14 (42.9%) MEST by next-generation sequencing (N=5) and karyotype (N=1). Relative whole-chromosome gains of chromosome 12 were identified in 5/14 (35.7%) MESTs. Two cases showed gains on chromosome 12 alone. Three cases with chromosome 12 gains harbored additional nonrecurrent CNAs. A single case without chromosome 12 gain harbored a relative whole-chromosome gain of chromosome 8 and loss of chromosome 21. No clinically actionable alterations were identified, and there were no alterations in renal neoplasia-related genes (eg, VHL, FH, SDHA/B/D, ELOC, TFEB, TFE3, DICER1, MET, MTOR, and TSC1/2). Of 13 cases with follow-up (median: 81.2 mo), no recurrences were identified after surgery. Although not entirely sensitive nor specific, chromosome 12 gain is the first evidence of recurrent alterations in MEST, supporting its classification as a neoplasm.
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