Simultaneous Adrenocortical Carcinoma and Neuroblastoma in an Infant With a Novel Germline p53 Mutation
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Oncology,Hematology,Pediatrics, Perinatology, and Child Health
Reference24 articles.
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2. . Are there low-penetrance TP53 alleles Evidence from childhood adrenocortical tumors.;Varley;Am J Med Genet,1999
3. Li-fraumeni syndrome.;Malkin;Genes Cancer,2011
4. . Relative frequency and morphology of cancers in carriers of germline TP53 mutations.;Birch;Oncogene,2001
5. . Beyond Li Fraumeni syndrome: clinical characteristics of families with p53 germline mutations.;Gonzalez;J Clin Oncol,2009
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1. Characteristics of Adrenocortical Carcinoma Associated With Lynch Syndrome;The Journal of Clinical Endocrinology & Metabolism;2020-11-13
2. A case of synchronous malignancy with novel missense mutation in a child: Is this Li-Fraumeni syndrome or a novel case masquerading as Li-Fraumeni syndrome??;Indian Journal of Medical and Paediatric Oncology;2020-09
3. Synchronous adrenocortical carcinoma and rhabdomyosarcoma in a child with p53 Overexpression on immunostaining;Pediatric Hematology Oncology Journal;2020-09
4. Co-Occurrence of Adrenocortical Carcinoma and Gastrointestinal Stromal Tumor in a Patient with Neurofibromatosis Type 1 and a History of Endometrial Cancer;Acta Endocrinologica (Bucharest);2020
5. Composite Adrenocortical Carcinoma and Neuroblastoma in an Infant With a TP53 Germline Mutation: A Case Report and Literature Review;Journal of Pediatric Hematology/Oncology;2019-07
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