Article

Composite Adrenocortical Tumor and Neuroblastoma in an Infant with a Heterozygous TP53 Germline Mutation

2024-01-31

Abstract excerpt

Composite malignancy of both Li Fraumeni syndrome (LFS) associated adrenocortical tumor (ACT) and neuroblastoma (NB) is extremely rare. We report a 10-month-old boy with a right sided abdominal mass that, after multiple resections, noted two separate tumors. The adrenal resection revealed characteristics notable for an ACT; the para-aortic and pelvic lymph nodes showed poorly differentiated NB. Additional analysis...

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Literature Corpus work: a003fa8d-5d96-59b0-994b-951dbffbed01
DOI: 10.22541/au.170670445.55190323/v1

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