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2.
BMJ Case Rep ; 15(2)2022 Feb 09.
Artigo em Inglês | MEDLINE | ID: mdl-35140090

RESUMO

Rhinosporidiosis is a chronic mucocutaneous granulomatous disease caused by Rhinosporidium seeberi, commonly affecting the nose and nasopharynx. Endobronchial involvement is of rare occurrence but can pose challenging problems for diagnosis, surgical excision and anaesthetic management. We report a 40-year-old man with a history of recurrent nasal rhinosporidiosis who presented with unilateral nasal obstruction, cough, shortness of breath and a radiological feature of left lung collapse. Eight years since the last surgery, he presented with a recurrent lesion in the nose with concurrent endobronchial involvement. The patient underwent excision of the nasal and the endobronchial lesion successfully under general anaesthesia without any complication and good symptomatic improvement. The clinical presentation and the management of endobronchial rhinosporidiosis are discussed here. The surgical difficulties faced during the procedure are highlighted.


Assuntos
Obstrução Nasal , Rinosporidiose , Adulto , Animais , Brônquios , Humanos , Masculino , Obstrução Nasal/etiologia , Obstrução Nasal/cirurgia , Nariz , Rinosporidiose/diagnóstico por imagem , Rinosporidiose/cirurgia , Rhinosporidium
3.
BMJ Case Rep ; 15(2)2022 Feb 07.
Artigo em Inglês | MEDLINE | ID: mdl-35131785

RESUMO

Bleeding nasal mass in adolescent boys has customarily been attributed to Juvenile nasopharyngeal angiofibroma. However, little is known regarding the extranasopharyngeal origin of angiofibroma, as highlighted in this case report of a 15-year-old boy who presented with recurrent epistaxis and nasal obstruction. On constructing a working diagnosis of nasal haemangioma, the patient was taken up for endoscopic excision under general anaesthesia. Intraoperative endoscopic findings and histopathological examination revealed the diagnosis of middle turbinate angiofibroma, which is an extremely rare extranasopharyngeal angiofibroma. Consequently, this represents the third described case of a juvenile angiofibroma arising from the middle turbinate.


Assuntos
Angiofibroma , Obstrução Nasal , Neoplasias Nasofaríngeas , Neoplasias Nasais , Adolescente , Angiofibroma/diagnóstico por imagem , Angiofibroma/cirurgia , Humanos , Masculino , Obstrução Nasal/etiologia , Obstrução Nasal/cirurgia , Neoplasias Nasofaríngeas/diagnóstico por imagem , Neoplasias Nasofaríngeas/cirurgia , Neoplasias Nasais/diagnóstico por imagem , Neoplasias Nasais/cirurgia , Conchas Nasais/diagnóstico por imagem , Conchas Nasais/cirurgia
4.
Indian J Otolaryngol Head Neck Surg ; 74(Suppl 3): 6170-6173, 2022 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-36742934

RESUMO

Mucoepidermoid carcinoma is the most common salivary gland malignancy and about one third occurs in the parotid gland. The peak incidence is commonly seen between the third and fifth decades of life. It routinely presents as a fixed, painless mass below the ear. However, its presentation as a giant mass is exceedingly rare. Here, we report a case of a recurrent giant exophytic mucoepidermoid carcinoma in a young male. He underwent Revision Total Parotidectomy with Modified Radical neck dissection with Sural nerve grafting and an Anterolateral thigh flap reconstruction followed by Adjuvant radiotherapy. The rarity of the clinical presentation and the management challenges faced in a young male are being discussed in this case report.

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