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Surgical management of pediatric salivary malignant tumors-A single-center cohort study.
Lopez, Joseph; Chen, Yu Han; Eagan, Alana; Fitzgerald, Conall; Woods, Robbie; Wong, Richard; Shah, Jatin; Ganly, Ian.
Afiliação
  • Lopez J; Department of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
  • Chen YH; Division of Pediatric Head & Neck Surgery, AdventHealth For Children, Orlando, Florida, USA.
  • Eagan A; Department of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
  • Fitzgerald C; Department of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
  • Woods R; Department of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
  • Wong R; Department of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
  • Shah J; Department of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
  • Ganly I; Department of Surgery, Head & Neck Service, Memorial Sloan Kettering Cancer Center, New York City, New York, USA.
J Surg Oncol ; 126(8): 1389-1395, 2022 Dec.
Article em En | MEDLINE | ID: mdl-35969241
ABSTRACT

BACKGROUND:

The purpose of this study was to report incidence, clinicopathologic behavior, management, and outcome of pediatric patients treated surgically for salivary gland (SG) malignancies.

METHODS:

Patients who underwent surgery for SG malignancies from 1985 to 2015 were identified. Clinical, pathological, treatment and outcomes data were collected. Disease-specific survival (DSS), recurrence-free survival (RFS), and overall survival (OS) were calculated using Kaplan-Meier method.

RESULTS:

Twenty-eight pediatric patients were included. The most common histopathological types were mucoepidermoid (n = 18, 64.3%), acinic cell (n = 7, 25.0%), adenoid cystic (n = 2, 7.1%), and adenocarcinoma (n = 1, 3.6%). Surgical approach varied and ranged from superficial parotidectomy (n = 11, 39.3%) to partial maxillectomy (n = 6, 21.4%). Nine patients (32%) required postoperative radiotherapy. DSS, OS, and RFS probability at 5 years were 96.4%, 96.4%, and 89.3%, respectively.

CONCLUSION:

Pediatric SG malignancies are rare and have favorable outcome at 5 years. Larger, multi-institutional studies are required to better understand the natural history of these rare tumors.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias das Glândulas Salivares / Adenocarcinoma / Carcinoma Mucoepidermoide Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Revista: J Surg Oncol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias das Glândulas Salivares / Adenocarcinoma / Carcinoma Mucoepidermoide Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Revista: J Surg Oncol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos