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1.
Journal of Rhinology ; : 139-141, 2013.
Artigo em Inglês | WPRIM | ID: wpr-133773

RESUMO

In this paper, we report a case of bilateral inferior and middle turbinate agenesis, a rare anomaly. A 27-year-old woman presented with nasal obstruction, crust formation, anosmia, and foul odors. Anterior rhinoscopic examination revealed the absence of the middle and inferior turbinates on both sides. The patient had no history of nasal or sinus surgery. She denied over having expelled anything of significance from her nasal cavity. She had no history of infectious disease-including tuberculosis and syphilis, granuolomatous diseases, sarcoids, Wegener's disease, and radiation therapy. There have been few reports on bilateral turbinate agenesis.


Assuntos
Adulto , Feminino , Humanos , Cavidade Nasal , Obstrução Nasal , Odorantes , Transtornos do Olfato , Rinite , Rinite Atrófica , Sífilis , Tuberculose , Conchas Nasais
2.
Journal of Rhinology ; : 139-141, 2013.
Artigo em Inglês | WPRIM | ID: wpr-133772

RESUMO

In this paper, we report a case of bilateral inferior and middle turbinate agenesis, a rare anomaly. A 27-year-old woman presented with nasal obstruction, crust formation, anosmia, and foul odors. Anterior rhinoscopic examination revealed the absence of the middle and inferior turbinates on both sides. The patient had no history of nasal or sinus surgery. She denied over having expelled anything of significance from her nasal cavity. She had no history of infectious disease-including tuberculosis and syphilis, granuolomatous diseases, sarcoids, Wegener's disease, and radiation therapy. There have been few reports on bilateral turbinate agenesis.


Assuntos
Adulto , Feminino , Humanos , Cavidade Nasal , Obstrução Nasal , Odorantes , Transtornos do Olfato , Rinite , Rinite Atrófica , Sífilis , Tuberculose , Conchas Nasais
3.
Korean Journal of Otolaryngology - Head and Neck Surgery ; : 465-468, 2013.
Artigo em Coreano | WPRIM | ID: wpr-645850

RESUMO

Langerhans cell histiocytosis (LCH) is a rare disease characterized by clonal proliferation of Langerhans cells. The temporal bone is frequently involved in pediatric LCH cases, but there have been few reports of adult LCH with temporal bone involvement. We present a case of adult onset LCH affecting the temporal bone. The diagnosis was made by biopsy, based on histopathologic findings of Langerhans cells. Diagnostic and therapeutic considerations of LCH involving the temporal bone are discussed.


Assuntos
Adulto , Humanos , Biópsia , Meato Acústico Externo , Histiocitose de Células de Langerhans , Células de Langerhans , Doenças Raras , Osso Temporal
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