Literature DB >> 18086819

Cancer of the nasal cavity in the pediatric population.

Margo McKenna Benoit1, Neil Bhattacharyya, William Faquin, Michael Cunningham.   

Abstract

OBJECTIVE: The purpose of this work was to investigate the clinical manifestations and diagnostic range of malignant entities presenting as a nasal mass in the pediatric population. PATIENTS AND METHODS: A retrospective cohort analysis was conducted at a specialty hospital and a tertiary care university hospital. Patients aged between birth and 18 years and diagnosed with a malignancy that arose within the nasal cavity between the years 1991 and 2006 were included. This institution-specific patient group was compared with a similar cohort of patients extracted from the national Surveillance Epidemiology and End Results database. The main outcome measures were the incidence, presentation, and diagnoses of nasal cancer presenting in this population.
RESULTS: Sixteen patients with nasal malignancies presented institutionally in the defined pediatric age group. Patient age at the time of diagnosis ranged from 7 months to 17 years, with a slight male predominance. The main presenting symptoms were unilateral nasal congestion and ophthalmologic complaints. The median time from presentation to diagnosis was 7 weeks; patients who presented with nonspecific complaints, such as nasal obstruction, headache, and fatigue, were given a diagnosis, on average, later than those who presented with focal manifestations. Nationwide, 47 patients were identified from the Surveillance Epidemiology and End Results database. In both subject groups, the most common diagnoses were rhabdomyosarcoma (37.5% institutionally and 23% in the Surveillance Epidemiology and End Results group) and esthesioneuroblastoma (25% institutionally and 28% Surveillance Epidemiology and End Results). In the Surveillance Epidemiology and End Results cohort, the overall mean survival rate was 188 months.
CONCLUSIONS: Nasal cancer in the pediatric population often presents with nonspecific signs and symptoms, and a high index of suspicion is necessary for a timely diagnosis. Soft tissue sarcomas are expectedly common. The relative high frequency of esthesioneuroblastoma is particularly noteworthy.

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Year:  2007        PMID: 18086819     DOI: 10.1542/peds.2007-1319

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  5 in total

1.  Esthesioneuroblastoma in pediatric and adolescent age. A report from the TREP project in cooperation with the Italian Neuroblastoma and Soft Tissue Sarcoma Committees.

Authors:  Gianni Bisogno; Pietro Soloni; Massimo Conte; Marta Podda; Andrea Ferrari; Alberto Garaventa; Roberto Luksch; Giovanni Cecchetto
Journal:  BMC Cancer       Date:  2012-03-25       Impact factor: 4.430

2.  Multimodality Treatment of Pediatric Esthesioneuroblastoma.

Authors:  Rajkumar Venkatramani; Hubert Pan; Wayne L Furman; Jonathan M Marron; Josephine Haduong; Paola Friedrich-Medina; Anita Mahajan; Abhishek Bavle; Hao Wu; Murali Chintagumpala
Journal:  Pediatr Blood Cancer       Date:  2015-10-30       Impact factor: 3.167

Review 3.  Esthesioneuroblastoma: Multimodal management and review of literature.

Authors:  Ritesh Kumar
Journal:  World J Clin Cases       Date:  2015-09-16       Impact factor: 1.337

Review 4.  An Update on Sinonasal Round Cell Undifferentiated Tumors.

Authors:  Alessandro Franchi
Journal:  Head Neck Pathol       Date:  2016-02-01

5.  Clinical manifestations of head and neck cancer in pediatric patients, an analysis of 253 cases in a single Brazilian center.

Authors:  L-P-A Arboleda; M-E Pérez-de-Oliveira; I-L Hoffmann; I-A Cardinalli; K-P Gallagher; A-R Santos-Silva; R-M Mendonça
Journal:  Med Oral Patol Oral Cir Bucal       Date:  2022-05-01
  5 in total

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