Congenital nasal chondromesenchymal hamartoma
Philippine Journal of Otolaryngology Head and Neck Surgery
;
: 23-26, 2009.
Artigo
em Inglês
| WPRIM
| ID: wpr-633257
ABSTRACT
Objectives:
To report the case of a congenital nasal chondromesenchymal hamartoma in a oneyear- old female and review the literature, identifying problems encountered in confirming the diagnosis and in treatment of this patient.Methods:
Design:
Case ReportSetting:
Tertiary Public General Hospital Patient OneResults:
A one-year-old female with an intranasal mass noted at birth and with subsequent unilateral maxillary enlargement is described. Computed tomography showed calcifications and erosion of adjacent bony structures. Histopathology and immunohistochemistry of an intranasalbiopsy were interpreted as chordoma, a malignant tumor. Following surgical excision, the final histopathologic diagnosis was chondroid hamartoma.Conclusion:
Only 20 cases of nasal chondromesenchymal hamartoma have been reported in the literature worldwide. These tumors may present clinically, histopathologicaly and radiologically as malignant tumors and may mislead even the experts. The whole clinical picture should be taken together to avoid misdiagnosis as a malignancy and to facilitate appropriate management.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Tipo de estudo:
Estudo prognóstico
Idioma:
Inglês
Revista:
Philippine Journal of Otolaryngology Head and Neck Surgery
Ano de publicação:
2009
Tipo de documento:
Artigo
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