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A Case of Cervical Neuroblastoma Complained Chiefly with Stridor / 소아알레르기및호흡기학회지
Pediatric Allergy and Respiratory Disease ; : 327-333, 1999.
Artigo em Coreano | WPRIM | ID: wpr-106014
ABSTRACT
Primary cervical neuroblastoma is very rare disease in neonates and should be distinguished with other diseases, which cause stridor in neonate, including laryngomalacia, vocal cord paralysis, laryngeal web, laryngotracheal esophageal cleft, laryngotracheal stenosis, etc. It is characterized by cough, stridor, dysphagia, neck mass, Horner syndrome and heterochromia iridis. Survival rate is high even in the advanced cases, in which the residual mass is remained after partial resection, without further therapy. A 1-day-old girl showed severe dyspnea with inspiratory stridor after birth. At first, she was misdiagnosed as a case of laryngomalacia, but later proved to have stage I primary neuroblastoma by plain X-ray film of lateral view of the neck, flexible nasolaryngoscopy, and computerized tomography. She has been well without relapse after total resection for 1 (1/2) year. We report this case as the first case in Korea.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Recidiva / Filme para Raios X / Transtornos de Deglutição / Sons Respiratórios / Paralisia das Pregas Vocais / Síndrome de Horner / Taxa de Sobrevida / Constrição Patológica / Tosse / Doenças Raras Limite: Feminino / Humanos / Recém-Nascido País/Região como assunto: Ásia Idioma: Coreano Revista: Pediatric Allergy and Respiratory Disease Ano de publicação: 1999 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Recidiva / Filme para Raios X / Transtornos de Deglutição / Sons Respiratórios / Paralisia das Pregas Vocais / Síndrome de Horner / Taxa de Sobrevida / Constrição Patológica / Tosse / Doenças Raras Limite: Feminino / Humanos / Recém-Nascido País/Região como assunto: Ásia Idioma: Coreano Revista: Pediatric Allergy and Respiratory Disease Ano de publicação: 1999 Tipo de documento: Artigo