Literature DB >> 33314344

Clinicopathological analysis and survival outcomes of primary salivary gland tumors in pediatric patients: A systematic review.

Brendo Vinícius Rodrigues Louredo1, Alan Roger Santos-Silva1, Pablo Agustin Vargas1, Márcio Ajudarte Lopes1, Manoela Domingues Martins1,2, Eliete Neves da Silva Guerra3, Ana Carolina Prado Ribeiro1,4, Thaís Bianca Brandão4, Regina Maria Holanda de Mendonça5, Luiz Paulo Kowalski1,6,7, Paul M Speight8, Syed Ali Khurram8, Maria Eduarda Pérez-de-Oliveira1.   

Abstract

BACKGROUND: Salivary gland tumors are a diverse group of uncommon neoplasms that are rare in pediatric patients. The aim of this study was to evaluate the clinicopathological profile and survival outcomes of pediatric patients affected by salivary gland tumors.
MATERIALS AND METHODS: An extensive search was carried out using the MEDLINE/PubMed, EMBASE, Scopus databases, and grey literature. The risk of bias was available in all papers included.
RESULTS: A total of 2,830 articles were initially retrieved with 54 remaining for data extraction, resulting in 2,937 cases. This comprised forty-five case series' and nine cohort studies. These tumors were slightly more prevalent in females (57.4%). The patients' age ranged from 0.3 to 19 years old, with a mean age of 13.3 years. Parotid was the most affected site (81.9%), and 99.2% of cases clinically exhibited a swelling. Presence of pain/tenderness was reported in 13.5% of the cases, with an average duration of 12.6 months for the appearance of symptoms. Most of the reported cases were malignant tumors (75.4%), with mucoepidermoid carcinoma the most common tumor of all tumors (44.8%), followed by pleomorphic adenoma (24.1%). Surgery alone was the leading treatment choice in 74.9% cases, and the 5-year overall survival rate of patients was 93.1%. Patients with symptoms (P = .001), local recurrence (P < .001), metastasis (P < .001), and those not undergoing surgery or surgery combined with radiotherapy (P < .001) showed lower survival rates.
CONCLUSION: The pediatric patients present a high frequency of malignant salivary neoplasms and a high overall survival rate.
© 2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  mucoepidermoid carcinoma; pediatric; prognosis; salivary gland neoplasms; survival

Year:  2021        PMID: 33314344     DOI: 10.1111/jop.13151

Source DB:  PubMed          Journal:  J Oral Pathol Med        ISSN: 0904-2512            Impact factor:   4.253


  2 in total

1.  Morphologic and Ancillary Studies of Pediatric Acinic Cell Carcinoma: A Single Institute Experience.

Authors:  Grayson G Cole; Cláudia M Salgado; Danielle Vargas de Stefano; Eduardo V Zambrano; Ana M Gómez; Miguel Reyes-Múgica; Qian Wang
Journal:  Head Neck Pathol       Date:  2022-09-28

2.  Indications and Outcomes of Parotidectomy in Saudi Children: Experience From Two Tertiary Centers.

Authors:  Ahmad Albosaily; Turki Aldrees; Saleh Aldhahri; Khalid Al-Qahtani
Journal:  Cureus       Date:  2021-11-15
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.