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2.
J Mycol Med ; 24(2): 171-4, 2014 Jun.
Artigo em Francês | MEDLINE | ID: mdl-24746718

RESUMO

INTRODUCTION: Sinonasal aspergillosis is caused by the interaction between the sinonasal mucosa with a cosmopolite fungus (Aspergillus), it is on the increase, this is an infection whose evolution is unpredictable requiring early diagnosis and appropriate support. We report a case of Aspergillus rhinosinusitis of dental origin in pseudo-tumoral form with a review of the literature. CLINICAL CASE: A 31 years-old, women, consulted for a right nasal obstruction with purulent rhinorrhea after dental treatment. On examination, there was a bulge of the inner canthus of the right eye and a mass in the right nasal cavity. The CT scanner showed a process of the left naso-sinus cavity centered by calcic image density. The patient underwent a total excision of the mass endoscopically. Mycological and pathological examination concluded that the etiology was Aspergillus fumigatus. The patient had not received any antifungal treatment. The postoperative course was uneventful. The evolution was favourable with no recurrence after 9 months. DISCUSSION: Aspergillus rhinosinusitis of dental origin is usually due to the emergence of canalicular filling paste into the maxillary sinus through and oral cavity and sinus fistula, neglected it can progress to invasive pseudo-tumoral form. The clinical presentation is nonspecific and the diagnosis often involves imaging (scanner). Mycological and histological examinations are essential for diagnosis. The treatment is based on surgery sometimes associated with antifungal treatment.


Assuntos
Aspergilose/diagnóstico , Aspergillus fumigatus , Fístula Dentária/microbiologia , Rinite/microbiologia , Sinusite/microbiologia , Abscesso/complicações , Abscesso/diagnóstico , Abscesso/microbiologia , Adulto , Aspergilose/complicações , Aspergilose/microbiologia , Aspergillus fumigatus/isolamento & purificação , Fístula Dentária/complicações , Feminino , Humanos , Doenças Maxilares/complicações , Doenças Maxilares/diagnóstico , Doenças Maxilares/microbiologia , Obstrução Nasal/microbiologia , Pólipos Nasais/complicações , Pólipos Nasais/diagnóstico , Pólipos Nasais/microbiologia , Rinite/complicações , Sinusite/complicações
3.
Case Rep Otolaryngol ; 2012: 262958, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22953104

RESUMO

The posttraumatic cholesteatoma is a rare complication of different types of the temporal bone damage. Its diagnosis is often done after several years of evolution, sometimes even at the stage of complications. A case of posttraumatic cholesteatoma is presented that was revealed by a facial nerve paralysis 23 years after a crash of the external auditory canal underlining the importance of the otoscopic and radiological regular monitoring of the patients with a traumatism of the temporal bone.

4.
Rev Stomatol Chir Maxillofac ; 112(5): 310-2, 2011 Nov.
Artigo em Francês | MEDLINE | ID: mdl-21940027

RESUMO

INTRODUCTION: Osler-Rendu-Weber syndrome is an inherited disorder characterized by mucocutaneous and visceral telangiectasia. It is often revealed by recurrent epistaxis. It is sometimes profuse and intractable. Hemostasis may be problematic. CASE STUDY: A 61-year-old male patient presented with severe epistaxis due to Osler-Rendu-Weber syndrome. Embolization of the external carotid branches was needed for hemostasis. DISCUSSION: Embolization of external carotid artery branches can be an effective therapeutic alternative when usual treatments fail.


Assuntos
Epistaxe/etiologia , Telangiectasia Hemorrágica Hereditária/complicações , Embolização Terapêutica , Epistaxe/diagnóstico , Epistaxe/terapia , Humanos , Masculino , Pessoa de Meia-Idade , Índice de Gravidade de Doença , Telangiectasia Hemorrágica Hereditária/diagnóstico , Telangiectasia Hemorrágica Hereditária/terapia
5.
Rev Stomatol Chir Maxillofac ; 112(3): 177-9, 2011 Jun.
Artigo em Francês | MEDLINE | ID: mdl-21429542

RESUMO

INTRODUCTION: A leiomyosarcoma is a malignant tumor of the smooth muscle. Its malignancy is difficult to assess. Submandibular gland involvement is extremely rare. OBSERVATION: A 62-year-old patient was admitted with a primary leiomyosarcoma of the submandibular gland. He was treated by surgery and radiotherapy. The patient died 11 months later from pulmonary metastases. DISCUSSION: LMS of the submandibular gland is extremely rare. Its diagnosis is very difficult because of the non-specific clinical and radiological signs. The histological diagnosis often relies on immunohistochemistry. Treatment is based on surgery associated to radiotherapy. The prognosis remains poor because of frequent recurrence and metastases.


Assuntos
Leiomiossarcoma/diagnóstico , Neoplasias da Glândula Submandibular/diagnóstico , Evolução Fatal , Humanos , Leiomiossarcoma/secundário , Leiomiossarcoma/cirurgia , Neoplasias Pulmonares/secundário , Excisão de Linfonodo , Masculino , Pessoa de Meia-Idade , Terapia Neoadjuvante , Radioterapia Adjuvante , Neoplasias da Glândula Submandibular/cirurgia
6.
Ann Endocrinol (Paris) ; 70(4): 256-60, 2009 Sep.
Artigo em Francês | MEDLINE | ID: mdl-19591972

RESUMO

Cysts of the thyroglossal duct are common but malignant degeneration is rare, occurring only in 1% of the cases. The most frequent histological type is papillary carcinoma. The clinical presentation of these cancers is generally nonspecific, diagnosis being established postoperatively using the Sistrunk method. Debate remains open concerning appropriate management strategies and post-therapeutic follow-up for this type of neoplasia. We report the case of a 45-year-old patient who underwent surgery for an anterior neck mass that had developed over three years. Histology favored multifocal papillary carcinoma in a thyroglossal duct remant. Total thyroidectomy was performed. The postoperative protocol, established empirically due to the absence of consensus, included radioactive iodine and hormone suppression even though the thyroid was intact. After one year of follow-up, outcome has remained favorable.


Assuntos
Carcinoma Papilar/patologia , Neoplasias de Cabeça e Pescoço/patologia , Cisto Tireoglosso/patologia , Carcinoma Papilar/cirurgia , Neoplasias de Cabeça e Pescoço/cirurgia , Humanos , Masculino , Pessoa de Meia-Idade , Cisto Tireoglosso/cirurgia , Tireoidectomia , Resultado do Tratamento
7.
B-ENT ; 1(3): 145-9, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16255499

RESUMO

Laryngeal leiomyosarcoma is rare. The authors report the case of a 48-year-old patient who presented with progressive hoarseness. This symptomatology was associated with a laryngeal tumour. Immunohistopathological study indicated a leiomyosarcoma. Acute dyspnoea resulted in an urgent tracheostomy, followed by total laryngectomy without neck dissection later. In the light of this observation and a literature review, histopathological characteristics, clinical aspects and therapeutic indications will be discussed for this localisation.


Assuntos
Neoplasias Laríngeas/diagnóstico , Neoplasias Laríngeas/cirurgia , Leiomiossarcoma/diagnóstico , Leiomiossarcoma/cirurgia , Dispneia/etiologia , Feminino , Rouquidão/etiologia , Humanos , Neoplasias Laríngeas/complicações , Laringectomia , Leiomiossarcoma/complicações , Pessoa de Meia-Idade
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