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Surgical management of rare tumors (Part 1).
Stetson, Alyssa; Saluja, Saurabh; Cameron, Danielle B; Mansfield, Sara A; Polites, Stephanie F; Honeyman, Joshua N; Dahl, John P; Austin, Mary T; Aldrink, Jennifer H; Christison-Lagay, Emily R.
Afiliação
  • Stetson A; Department of Surgery, Division of Pediatric Surgery, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Saluja S; Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Cameron DB; Department of Surgery, Division of Pediatric Surgery, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Mansfield SA; Division of General Pediatric Surgery, Nationwide Children's Hospital, Columbus, Ohio, USA.
  • Polites SF; Division of Pediatric Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Honeyman JN; Division of Pediatric Surgery, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Dahl JP; Division of Otolaryngology, Division of Pediatric Otolaryngology, Seattle Children's Hospital, University of Washington, Seattle, Washington, USA.
  • Austin MT; Department of Pediatric Surgery, University of Texas Health Science Center at Houston and Department of Surgical Oncology and Pediatrics, UT MD Anderson Cancer Center, Houston, Texas, USA.
  • Aldrink JH; Division of General Pediatric Surgery, Nationwide Children's Hospital, Columbus, Ohio, USA.
  • Christison-Lagay ER; Division of Pediatric Surgery, Yale School of Medicine, Yale-New Haven Hospital, New Haven, Connecticut, USA.
Pediatr Blood Cancer ; : e31287, 2024 Aug 26.
Article em En | MEDLINE | ID: mdl-39185712
ABSTRACT
With an annual cumulative occurrence of approximately 15,000 in North America, all childhood cancers are rare. Very rare cancers as defined by both the European Cooperative Study Group for Rare Pediatric Cancers and the Children's Oncology Group fall into two principal categories those so uncommon (fewer than 2 cases/million) that their study is challenging even through cooperative group efforts (e.g., pleuropulmonary blastoma and desmoplastic small round cell tumor) and those that are far more common in adults and therefore rarely studied in children (e.g., thyroid, melanoma, and gastrointestinal stromal tumor). Treatment strategies for these latter tumors are typically based on adult guidelines, although the pediatric variants of these tumors may harbor different genetic signatures and demonstrate different behavior. If melanoma and differentiated thyroid cancer are excluded, other rare cancer types account for only 2% of the cancers in children aged 0 to 14. This article highlights several of the most common rare tumor types.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pediatr Blood Cancer Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pediatr Blood Cancer Ano de publicação: 2024 Tipo de documento: Article