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2.
Ear Nose Throat J ; 91(9): E4-6, 2012 Sep.
Article de Anglais | MEDLINE | ID: mdl-22996719

RÉSUMÉ

Metaplasia is the conversion of one adult tissue or cell type into another tissue or cell type. Although osseous metaplasia has been described in many parts of the body, it is rarely encountered in the head and neck region, especially in nasal polyps. This article reports a case of unilateral sinonasal polyp containing areas of osseous metaplasia in a 44-year-old woman presenting with nasal obstruction. Also included are a brief discussion of osseous metaplasia in the head and neck region and a literature review.


Sujet(s)
Polypes du nez/diagnostic , Ossification hétérotopique/diagnostic , Adulte , Angiofibrome/diagnostic , Diagnostic différentiel , Femelle , Humains , Métaplasie , Mycoses/diagnostic , Polypes du nez/anatomopathologie , Ossification hétérotopique/anatomopathologie , Papillome inversé/diagnostic , Sinusite/diagnostic
3.
J Craniofac Surg ; 22(3): 1134-6, 2011 May.
Article de Anglais | MEDLINE | ID: mdl-21586968

RÉSUMÉ

Basal cell carcinoma (BCC) is the most common skin cancer with a high propensity for local recurrence. The incidence of metastases from BCC is rare. We report a 65-year-old man who had BCC of the medial canthus of the left eye. In the 10-year period, he had been operated on approximately 12 times because of local recurrences. Three years after the last operation, he had a suspicious lesion on the operated area and a lumbar pain. Radiologic examination showed multiple metastatic skeletal and liver lesions. He was referred to the oncology department for radiation therapy and chemotherapy.


Sujet(s)
Carcinome basocellulaire/secondaire , Tumeurs de la paupière/anatomopathologie , Tumeurs du foie/secondaire , Tumeurs du rachis/secondaire , Sujet âgé , Cytoponction , Carcinome basocellulaire/chirurgie , Tumeurs de la paupière/chirurgie , Humains , Imagerie par résonance magnétique , Mâle , Tomographie par émission de positons , Tomodensitométrie
4.
J Craniofac Surg ; 21(4): 1290-1, 2010 Jul.
Article de Anglais | MEDLINE | ID: mdl-20647839

RÉSUMÉ

Epidermal inclusion cyst is a benign cyst filled with keratin fibers, and its wall has nearly the same characteristics as the epidermis. It is commonly seen in the skin and has the tendency to slowly grow toward deeper epidermis parts and to cause cystic expansion. We report a 23-year-old woman who presented with right external otitis lasting for 2 months. The patient's complaints did not respond to treatment even after parenteral antibiotic therapy. Surgical exploration revealed epidermal inclusion cyst of the ear canal. This pathologic entity is discussed in the light of current literature.


Sujet(s)
Conduit auditif externe/anatomopathologie , Kyste épidermique/anatomopathologie , Otite externe/anatomopathologie , Conduit auditif externe/chirurgie , Kyste épidermique/chirurgie , Femelle , Humains , Otite externe/chirurgie , Jeune adulte
5.
J Craniofac Surg ; 21(4): 1296-8, 2010 Jul.
Article de Anglais | MEDLINE | ID: mdl-20647842

RÉSUMÉ

In otolaryngology practice, we see young children who have inserted a foreign body (FB), which is usually found at home, into their ears or nose. Uncommon complications of an ingested FB are penetration and migration into the neck. Interestingly, among such FBs, sharp fish bones are the most commonly observed in Turkey. In our patient, the FB caused deep neck infection because of FB reaction. In our patient, we could not find any clue of a FB during examination. We were able to see the FB by magnetic resonance imaging (MRI). Interestingly, the FB looked like a carotid sheath on the MR image.


Sujet(s)
Corps étrangers/diagnostic , Corps étrangers/chirurgie , Cou , Enfant , Diagnostic différentiel , Corps étrangers/complications , Humains , Imagerie par résonance magnétique , Mâle
6.
J Craniofac Surg ; 21(1): 261-2, 2010 Jan.
Article de Anglais | MEDLINE | ID: mdl-20098193

RÉSUMÉ

Hypoglossal schwannoma is a rarely encountered skull base lesion that has generally both intracranial and extracranial parts. This article reports a case of hypoglossal schwannoma that is purely extracranial and presents itself only with persistent headache. Magnetic resonance imaging delineated a mass at the skull base that consisted of both cystic and solid components, consistent with a nerve sheath tumor. Cervical approach was chosen, and the mass was completely removed. Postoperatively, the patient developed hypoglossal nerve palsy because the hypoglossal nerve was sacrificed. Hypoglossal schwannomas are briefly discussed with a literature review.


Sujet(s)
Tumeurs des nerfs crâniens/complications , Céphalée/étiologie , Atteintes du nerf hypoglosse/complications , Neurinome/complications , Adulte , Tumeurs des nerfs crâniens/diagnostic , Tumeurs des nerfs crâniens/chirurgie , Diagnostic différentiel , Femelle , Humains , Atteintes du nerf hypoglosse/diagnostic , Atteintes du nerf hypoglosse/chirurgie , Imagerie par résonance magnétique , Neurinome/diagnostic , Neurinome/chirurgie
7.
Dysphagia ; 25(3): 258-60, 2010 Sep.
Article de Anglais | MEDLINE | ID: mdl-19784701

RÉSUMÉ

The case of a 29-year-old patient with active laryngeal tuberculosis predominantly involving the epiglottis, without pulmonary disease, is presented. The predominant symptoms are dysphagia, odynophagia, and hoarseness. Laryngeal carcinoma, which shares almost the same symptoms and signs, should be ruled out immediately. Laryngeal tuberculosis is discussed with a brief literature review.


Sujet(s)
Antituberculeux/usage thérapeutique , Épiglotte/microbiologie , Tuberculose laryngée/diagnostic , Adulte , Humains , Mâle , Mycobacterium tuberculosis , Tuberculose laryngée/traitement médicamenteux , Tuberculose laryngée/microbiologie
8.
Kulak Burun Bogaz Ihtis Derg ; 19(2): 103-5, 2009.
Article de Anglais | MEDLINE | ID: mdl-19796009

RÉSUMÉ

Neck abscess and deep neck infections are common diseases. Primary head and neck cancers may present initially with neck abscesses or deep neck infections. This presentation leads to delay of the diagnosis of underlying cancer. Head and neck cancers which present with deep neck infection initially have rarely been described. We report a case with relapsing deep neck infection who was diagnosed as proximal esophagus squamous cell carcinoma thereafter.


Sujet(s)
Abcès/étiologie , Carcinome épidermoïde/diagnostic , Tumeurs de l'oesophage/diagnostic , Infections/diagnostic , Antibactériens/usage thérapeutique , Carcinome épidermoïde/imagerie diagnostique , Céphalosporines/usage thérapeutique , Vertèbres cervicales/imagerie diagnostique , Tumeurs de l'oesophage/imagerie diagnostique , Femelle , Humains , Infections/étiologie , Infections à Klebsiella/diagnostic , Infections à Klebsiella/traitement médicamenteux , Adulte d'âge moyen , Nécrose , Récidive , Tomodensitométrie
9.
J Craniofac Surg ; 20(4): 1292-4, 2009 Jul.
Article de Anglais | MEDLINE | ID: mdl-19625853

RÉSUMÉ

Arteriovenous malformation is a tumor characterized by direct connection between an artery and vein without capillaries in-between, and it is commonly located intracranially. Intramuscular arteriovenous malformations are rare in the head and neck region. Less than 1% of the vascular tumors are localized in a muscle, 15% of them are in the head and neck muscles. Among the head and neck muscles, masseter muscle is the most common location, with the rate of 4.9%. The condition of a 36-year-old patient who applied to our clinic with the complaints of progressively increasing pain and progressively growing mass in the right cheek that appeared 1.5 years ago was diagnosed as arteriovenous malformation located in the masseter muscle. After preoperative embolization, the mass was successfully treated with total excision. In this case report, diagnostic and therapeutic tools addressing arteriovenous malformation located in the masseter muscle are discussed in the light of current literature.


Sujet(s)
Malformations artérioveineuses/chirurgie , Muscle masséter/chirurgie , Adulte , Malformations artérioveineuses/diagnostic , Angiographie cérébrale , Diagnostic différentiel , Embolisation thérapeutique , Humains , Imagerie par résonance magnétique , Mâle
10.
J Craniofac Surg ; 20(4): 1202-3, 2009 Jul.
Article de Anglais | MEDLINE | ID: mdl-19553838

RÉSUMÉ

Beckwith-Wiedemann syndrome is a congenital syndrome with some anomaly in overgrowth. Most common manifestations are exomphalos, macroglossia, gigantism, and visceromegaly. Overgrowth in tongue's size caused clinical symptoms such as dysphagia, speech disorder, strong in chewing, upper-airway obstruction, and psychological problems with appearance. Cold surgical techniques are commonly used in treating macroglossia. We presented tongue reduction with laser and its early result on a child with Beckwith-Wiedemann syndrome for macroglossia.


Sujet(s)
Syndrome de Beckwith-Wiedemann/chirurgie , Thérapie laser/méthodes , Langue/chirurgie , Dioxyde de carbone , Enfant , Humains , Mâle
11.
J Craniofac Surg ; 20(4): 1163-4, 2009 Jul.
Article de Anglais | MEDLINE | ID: mdl-19553847

RÉSUMÉ

Most preauricular masses are parotid neoplasms; however, some infectious and inflammatory causes may exhibit similar presentation. Toxoplasmosis is a worldwide parasitary disease. The clinical presentation of toxoplasmosis is mostly asymptomatic and may include subfebrile fever, fatigue, and lymphadenopathy. Only 13 clinical reports of intraglandular toxoplasmic lymphadenitis have been previously reported in the English literature. A careful history and examination with appropriate investigations, including immunoglobulin G avidity assay, will frequently provide the diagnosis of intraparotid toxoplasmosis. Surgery might therefore have been delayed or avoided depending on a satisfactory clinical improvement in consequence of proper medical treatment.


Sujet(s)
Lymphadénite/parasitologie , Maladies de la glande parotide/parasitologie , Toxoplasmose/diagnostic , Biopsie , Femelle , Humains , Lymphadénite/chirurgie , Adulte d'âge moyen , Maladies de la glande parotide/chirurgie , Toxoplasmose/complications , Toxoplasmose/chirurgie
12.
J Craniofac Surg ; 20(3): 930-5, 2009 May.
Article de Anglais | MEDLINE | ID: mdl-19461334

RÉSUMÉ

PURPOSE: To identify misdiagnostic points of hemangiopericytomas (HPs) of the head and neck. PATIENTS AND METHODS: We reviewed our clinical records from 2000 to 2007 retrospectively and identified 5 patients with HP of the head and neck. The records of each patient with head and neck HP were evaluated for age, sex, location of primary, clinical course, treatment, and tumor embolization (if performed). Pathologic slides of all patients were reviewed to identify histologic features and correlation with the clinical course and outcome for each lesion. RESULTS: Five patients with HP that arose from head and neck sites were identified. Five patients included 3 women and 2 men aged 9 to 52 years, with an average of 33.2 years. Each lesion of the patients derived from different parts of the head and neck. The most common complaints were painless mass (3 of 5) and nasal airway obstruction (3 of 5). Magnetic resonance imaging of the 3 patients reflected hyperintense on T2-weighted imaging and hypointense on T1-weighted imaging with diffuse enhancement after intravenous administration of gadolinium. Angiography was performed to all these 3 patients, and only 1 patient with cranial HP involvement did not show significant vascularity. Two patients had preoperative histopathologic results. All patients were operated on with appropriate approach. Pathologic slides of all patients were investigated and graded according to the tumor diameter, cellularity, mitotic rate, and necrosis. CONCLUSION: Differential diagnosis of clinical features and radiologic and pathologic aspects must be managed more carefully. Diagnostic way of these tumors has different pitfalls for the clinician.


Sujet(s)
Tumeurs de la tête et du cou/diagnostic , Hémangiopéricytome/diagnostic , Adolescent , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Angiographie , Biopsie , Enfant , Produits de contraste , Diagnostic différentiel , Embolisation thérapeutique , Femelle , Études de suivi , Gadolinium , Tumeurs de la tête et du cou/chirurgie , Hémangiome capillaire/diagnostic , Hémangiopéricytome/chirurgie , Humains , Amélioration d'image , Imagerie par résonance magnétique , Mâle , Méningiome/diagnostic , Adulte d'âge moyen , Obstruction nasale/diagnostic , Études rétrospectives , Résultat thérapeutique , Jeune adulte
13.
J Craniofac Surg ; 19(6): 1707-10, 2008 Nov.
Article de Anglais | MEDLINE | ID: mdl-19098590

RÉSUMÉ

Vocal cord paralysis and goiter are 2 common problems encountered in otolaryngology practice. Their coexistence, however, should arouse suspicion of the presence of malignant thyroid disease. Primary tracheal cancer is uncommon, and its incidence is very low compared with laryngeal cancer. Primary tracheal tumors can cause recurrent nerve palsy. We report here a rare case of vocal cord paralysis caused by a clinically occult tracheal squamous cell carcinoma in an 80-year-old patient with coincidental huge multinodular goiter.


Sujet(s)
Carcinome épidermoïde/diagnostic , Tumeurs des nerfs crâniens/diagnostic , Goitre nodulaire/complications , Nerf laryngé récurrent/anatomopathologie , Tumeurs de la trachée/diagnostic , Sujet âgé de 80 ans ou plus , Cytoponction , Carcinome épidermoïde/anatomopathologie , Tumeurs des nerfs crâniens/anatomopathologie , Femelle , Études de suivi , Humains , Imagerie par résonance magnétique , Invasion tumorale , Tomodensitométrie , Tumeurs de la trachée/anatomopathologie , Trachéomalacie/étiologie , Paralysie des cordes vocales/étiologie
14.
Oral Maxillofac Surg ; 12(3): 173-6, 2008 Sep.
Article de Anglais | MEDLINE | ID: mdl-18654805

RÉSUMÉ

INTRODUCTION: Chondrosarcomas of the mandible affecting the infratemporal fossa are very rare malignant tumors. DISCUSSION: In this article, two cases of chondrosarcoma invading the infratemporal fossa are presented, and clinical, histopathologic features, and therapeutic approaches are discussed, reviewing the literature.


Sujet(s)
Chondrosarcome/anatomopathologie , Tumeurs de la mandibule/anatomopathologie , Adulte , Fosse crânienne moyenne/anatomopathologie , Femelle , Humains , Mâle , Tumeurs de la base du crâne/anatomopathologie
15.
J Craniofac Surg ; 18(1): 241-3, 2007 Jan.
Article de Anglais | MEDLINE | ID: mdl-17251873

RÉSUMÉ

Synovial chondromatosis is a benign pathologic lesion that is considered to be a metaplastic process. This disease is rarely encountered in the temporomandibular joint (TMJ). In this article, a 72-year-old patient with synovial chondromatosis of the TMJ extending to the infratemporal fossa is presented and the literature is reviewed.


Sujet(s)
Chondromatose synoviale/anatomopathologie , Troubles de l'articulation temporomandibulaire/anatomopathologie , Articulation temporomandibulaire/anatomopathologie , Sujet âgé , Chondromatose synoviale/complications , Chondromatose synoviale/chirurgie , Femelle , Perte d'audition/étiologie , Humains , Articulation temporomandibulaire/chirurgie , Troubles de l'articulation temporomandibulaire/chirurgie
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