RÉSUMÉ
PURPOSE: We aimed to study reported cases of nasopharyngeal carcinoma presenting with ophthalmic manifestations with and without a prior diagnosis of nasopharyngeal carcinoma. METHODS: We conducted a systematic review following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). A literature search was conducted using the MEDLINE database in PubMed and Google Scholar. We included patients with a previous diagnosis of nasopharyngeal carcinoma in Group I and those without a prior diagnosis of nasopharyngeal carcinoma in Group II. Data included demographics, clinical presentation, history of nasopharyngeal carcinoma, treatment, histopathological description, World Health Organization classification, and outcome. RESULTS: Fifty-eight patients (26 in Group I and 32 in Group II) were included. The male-to-female ratio was 3:1. The mean age of the patients (53.3 ± 11.7 years and 54.8 ± 16.2 years, respectively) and gender did not differ significantly between the two groups. The most common ocular presentations were diplopia and proptosis in the first group (each in 34.6%), whereas visual disturbance was most common in the second group (46.9%). Treatment options and World Health Organization grading were comparable. The outcome in 38 patients (after a comparable follow-up period) was significantly better in group II (p=0.003). There was no statistically significant difference in the outcome of 23 patients in correlation with World Health Organization grades II versus III irrespective of group (p=0.094). CONCLUSIONS: The demographics of patients with nasopharyngeal carcinoma presenting with ophthalmic manifestations were similar between the two study groups, with a wide age range and male predominance. Patients presenting initially to ophthalmologists with no history of nasopharyngeal carcinoma have a more favorable outcome. World Health Organization grading may have less value as a prognostic indicator.
Sujet(s)
Exophtalmie , Maladies de l'oeil , Cancer du nasopharynx , Tumeurs du rhinopharynx , Humains , Bases de données factuelles , Exophtalmie/étiologie , Oeil , Cancer du nasopharynx/complications , Tumeurs du rhinopharynx/complications , Maladies de l'oeil/étiologieRÉSUMÉ
This study sought to identify and characterize the function of genes as diagnostic markers for Epstein-Barr virus (EBV)-related nasopharyngeal cancer (NPC). The gene expression profile of GSE13597 was downloaded from the Gene Expression Omnibus database, which included 28 EBV-related NPC gene expression profile data sets, 25 disease samples, and 3 control samples. Data were pre-processed, and differentially expressed genes were screened using the R language. The co-expression coefficient was calculated to construct a co-expression network using Cytoscape. ClusterONE was used to perform module analysis to find enriched gene families. The BiCAT software was used to perform a two-way clustering analysis of differentially expressed gene expression profiles based on the co-expression networks and to verify the enriched gene families, followed by functional enrichment analysis of these gene families. The MCM gene family was found to be enriched in EBV-related NPC. This gene family is essential for eukaryotic DNA replication. Functional analysis of differentially expressed genes in the co-expression network revealed that the enriched biological processes and pathways were mainly involved in the cell cycle. EBV-related NPC is likely associated mainly with the process of cell reproduction, providing a strong basis for the prevention, diagnosis, and treatment of EBV-related NPC and a direction for targeted chemotherapy.
Sujet(s)
Infections à virus Epstein-Barr/génétique , Régulation de l'expression des gènes tumoraux , Herpèsvirus humain de type 4/pathogénicité , Tumeurs du rhinopharynx/virologie , Analyse de regroupements , Infections à virus Epstein-Barr/complications , Infections à virus Epstein-Barr/anatomopathologie , Infections à virus Epstein-Barr/virologie , Analyse de profil d'expression de gènes , Herpèsvirus humain de type 4/génétique , Humains , Tumeurs du rhinopharynx/complications , Tumeurs du rhinopharynx/génétique , Tumeurs du rhinopharynx/anatomopathologieRÉSUMÉ
OBJECTIVES: To report the results of cochlear implantation via the middle fossa approach in 4 patients, discuss the complications, and present a detailed description of the programming specifications in these cases. STUDY DESIGN: Retrospective case review. SETTING: Tertiary-care referral center with a well-established cochlear implant program. PATIENTS: Four patients with bilateral canal wall down mastoid cavities who underwent the middle fossa approach for cochlear implantation. INTERVENTIONS: Cochlear implantation and subsequent rehabilitation. A middle fossa approach with cochleostomy was successfully performed on the most superficial part of the apical turn in 4 patients. A Nucleus 24 cochlear implant system was used in 3 patients and a MED-EL Sonata Medium device in 1 patient. The single electrode array was inserted through a cochleostomy from the cochlear apex and occupied the apical, middle, and basal turns. Telemetry and intraoperative impedance recordings were performed at the end of surgery. A CT scan of the temporal bones was performed to document electrode insertion for all of the patients. MAIN OUTCOME MEASURES: Complications, hearing thresholds, and speech perception outcomes were evaluated. RESULTS: Neural response telemetry showed present responses in all but 1 patient, who demonstrated facial nerve stimulation during the test. Open-set speech perception varied from 30% to 100%, despite the frequency allocation order of the MAP. CONCLUSION: Cochlear implantation via the middle cranial fossa is a safe approach, although it is a challenging procedure, even for experienced surgeons.
Sujet(s)
Implantation cochléaire/méthodes , Fosse crânienne moyenne/chirurgie , Perte d'audition/thérapie , Procédures de chirurgie otologique/méthodes , Adulte , Seuil auditif/physiologie , Chimioradiothérapie/effets indésirables , Cholestéatome de l'oreille moyenne/complications , Cholestéatome de l'oreille moyenne/chirurgie , Implantation cochléaire/effets indésirables , Fosse crânienne moyenne/anatomie et histologie , Maladies des oreilles/thérapie , Nerf facial/physiologie , Femelle , Surdité bilatérale partielle/chirurgie , Humains , Mâle , Mastoïde/chirurgie , Adulte d'âge moyen , Monitorage physiologique , Tumeurs du rhinopharynx/complications , Tumeurs du rhinopharynx/thérapie , Procédures de chirurgie otologique/effets indésirables , Complications postopératoires/thérapie , Études rétrospectives , Perception de la parole , Télémétrie , Os temporal/imagerie diagnostique , Tomodensitométrie , Résultat thérapeutiqueRÉSUMÉ
Juvenile nasopharyngeal angiofibroma (JNA) is a rare histologically benign tumor, highly vascularized, with usually aggressive behavior, and can extend from the nasal cavity to neighboring structures. We present the case of a 14-year-old male harboring a JNA, presenting with an active severe and persistent epistaxis. Two previous surgical attempts of removal were unsuccessful, because of profuse intraoperative bleeding. Angiography showed a highly vascularized neoplasm with multiple branches arising from both internal carotid arteries, with absence of branches from the external carotid due to previous surgical ligation. Direct puncture tumor embolization was not possible because removal of nasal packing triggered major hemorrhage. The only option for embolization was a technique of non-superselective embolization with particles under transient occlusion of the internal carotid artery. The procedure was performed uneventfully from either side, the tumor was subsequently removed, and the patient had no recurrence 2 years after the initial treatment.
Sujet(s)
Angiofibrome/thérapie , Occlusion par ballonnet , Perte sanguine peropératoire/prévention et contrôle , Artère carotide interne , Embolisation thérapeutique/méthodes , Tumeurs du rhinopharynx/thérapie , Hémorragie postopératoire/prévention et contrôle , Adolescent , Angiofibrome/vascularisation , Angiofibrome/complications , Angiofibrome/diagnostic , Angiofibrome/chirurgie , Angiographie de soustraction digitale , Épistaxis/étiologie , Humains , Imagerie par résonance magnétique , Mâle , Tumeurs du rhinopharynx/vascularisation , Tumeurs du rhinopharynx/complications , Tumeurs du rhinopharynx/diagnostic , Tumeurs du rhinopharynx/chirurgie , Hémorragie postopératoire/étiologie , Tomodensitométrie , Résultat thérapeutiqueRÉSUMÉ
Epignathus is a rare congenital nasopharyngeal tumour that is derived from the upper jaw, palate, and sphenoid bone. It usually protrudes through the mouth, leading to an appreciable risk of obstruction of the upper airway and death soon after birth. We report two cases of unusual presentations that illustrated some uncommon and similar characteristics. Although these tumours are not consistent in origin, number, and differentiation of tissues, both contained structures that were derived from all three layers of germ cells, including different anomalous tissues internally (dental bud, fat and muscular tissues, mucosal epithelium). Externally, they contained normal epidermis (skin with fine hairs). Imaging studies and operative findings showed that both tumours originated from the anterior portion of the sphenoid bone causing a sphenoidal sinus cleft without intracranial communication.
Sujet(s)
Tumeurs du rhinopharynx/anatomopathologie , Tératome/anatomopathologie , Fente palatine/complications , Femelle , Humains , Nouveau-né , Mâle , Tumeurs du rhinopharynx/complications , Tumeurs du rhinopharynx/chirurgie , Sinus sphénoïdal/anatomopathologie , Sinus sphénoïdal/chirurgie , Tératome/complications , Tératome/chirurgieRÉSUMÉ
OBJECTIVES: Juvenile nasopharyngeal angiofibroma is a rare benign tumor that affects young male patients and shows a characteristic development from its origin. It is not a true neoplasm, but shows features of vascular processes, developing into a more fibrous condition. The aim of this study was to correlate the clinical manifestations and the histologic findings of the tumor. METHODS: Thirty-six patients without previous treatment were studied. We correlated the incidence and duration of the clinical manifestations (nasal obstruction, epistaxis, nasal and/or pharyngeal tumor, and facial deformity) and morphometric histologic analyses of the central region of the tumor (number, caliber, and presence of muscle cells in the vessel wall, and tissue maturity and cellularity). RESULTS: The duration of nasal obstruction, the presence of nasal and/or pharyngeal tumor, and facial deformity were significantly correlated with the number of vessels, the tissue maturation, and the cellularity of the tumor. Epistaxis showed a strong correlation with the presence of muscle fibers in the vessels. CONCLUSIONS: There are correlations between the duration of the clinical manifestations and histologic maturation in the central portion of the tumor.
Sujet(s)
Angiofibrome/anatomopathologie , Tumeurs du rhinopharynx/anatomopathologie , Adolescent , Adulte , Angiofibrome/vascularisation , Angiofibrome/complications , Enfant , Épistaxis/étiologie , Humains , Mâle , Obstruction nasale/étiologie , Tumeurs du rhinopharynx/vascularisation , Tumeurs du rhinopharynx/complications , TomodensitométrieSujet(s)
Obstruction des voies aériennes/diagnostic , Exophtalmie/diagnostic , Lymphome B/diagnostic , Lymphome B diffus à grandes cellules/diagnostic , Tumeurs du rhinopharynx/diagnostic , Sujet âgé , Obstruction des voies aériennes/étiologie , Exophtalmie/étiologie , Issue fatale , Femelle , Humains , Lymphome B/complications , Lymphome B diffus à grandes cellules/complications , Tumeurs du rhinopharynx/complicationsSujet(s)
Femelle , Humains , Sujet âgé , Exophtalmie/diagnostic , Lymphome B diffus à grandes cellules , Lymphome B/diagnostic , Tumeurs du rhinopharynx/diagnostic , Obstruction des voies aériennes/diagnostic , Exophtalmie/étiologie , Issue fatale , Lymphome B diffus à grandes cellules , Lymphome B/complications , Tumeurs du rhinopharynx/complications , Obstruction des voies aériennes/étiologieSujet(s)
Femelle , Humains , Sujet âgé , Obstruction des voies aériennes/diagnostic , Exophtalmie/diagnostic , Lymphome B/diagnostic , Diagnostic/diagnostic , Tumeurs du rhinopharynx/diagnostic , Obstruction des voies aériennes/étiologie , Exophtalmie/étiologie , Issue fatale , Lymphome B/complications , /complications , Tumeurs du rhinopharynx/complicationsRÉSUMÉ
O padrão de múltiplas lesões pulmonares é uma apresentação radiológica comum em pessoas infectadas pelo HIV. As causas possíveis para este podem ser divididas dentro de duas categorias: infecções e neoplasias. Os autores descrevem o caso de um paciente de 53 anos de idade com carcinoma adenóide cístico de nasofaringe, múltiplos nódulos pulmonares e infecção pelo HIV
Sujet(s)
Humains , Mâle , Adulte d'âge moyen , Carcinome adénoïde kystique/complications , Infections à VIH/complications , Tumeurs du rhinopharynx/complications , Tumeurs du poumon/secondaire , Carcinome adénoïde kystique/diagnostic , Diagnostic différentiel , Tumeurs du rhinopharynx/diagnostic , Tumeurs du poumon/diagnosticRÉSUMÉ
Intermediate and highly malignant non-Hodgkin and primary central nervous system lymphomas are marker diseases for AIDS. Cavum and oropharynx involvement by these tumors is uncommon. Although there are few cases reported in the literature, these may be primary localizations of the tumor. We present a hemophilic HIV+ patient with non-Hodgkin lymphoma of the cavum. The histologic diagnosis was high-grade, pleomorphic, centroblastic lymphoma. The patient was treated with chemotherapy plus intrathecal chemotherapy and highly active antiretroviral therapy (HAART). His evolution has been excellent. One year after diagnosis, the patient is asymptomatic with no evidence of residual tumor, and responding well to HAART.
Sujet(s)
Syndrome d'immunodéficience acquise/complications , Hémophilie A/complications , Lymphome lié au SIDA/diagnostic , Lymphome malin non hodgkinien/diagnostic , Tumeurs du rhinopharynx/diagnostic , Adulte , Humains , Lymphome lié au SIDA/complications , Lymphome lié au SIDA/traitement médicamenteux , Lymphome malin non hodgkinien/complications , Lymphome malin non hodgkinien/traitement médicamenteux , Mâle , Tumeurs du rhinopharynx/complications , Tumeurs du rhinopharynx/traitement médicamenteux , TomodensitométrieSujet(s)
Humains , Mâle , Adulte , Hémophilie A/complications , Tumeurs du rhinopharynx/diagnostic , Lymphome malin non hodgkinien/diagnostic , Lymphome lié au SIDA/diagnostic , Syndrome d'immunodéficience acquise/complications , Lymphome lié au SIDA/complications , Lymphome lié au SIDA/traitement médicamenteux , Lymphome malin non hodgkinien/complications , Lymphome malin non hodgkinien/traitement médicamenteux , Tumeurs du rhinopharynx/complications , Tumeurs du rhinopharynx/traitement médicamenteux , TomodensitométrieSujet(s)
Humains , Mâle , Adulte , Hémophilie A/complications , Lymphome malin non hodgkinien/diagnostic , Lymphome lié au SIDA/diagnostic , Tumeurs du rhinopharynx/diagnostic , Syndrome d'immunodéficience acquise/complications , Lymphome malin non hodgkinien/complications , Lymphome malin non hodgkinien/traitement médicamenteux , Lymphome lié au SIDA/complications , Lymphome lié au SIDA/traitement médicamenteux , Tumeurs du rhinopharynx/complications , Tumeurs du rhinopharynx/traitement médicamenteux , TomodensitométrieRÉSUMÉ
The syndrome of inappropriate secretion of antidiuretic hormone (ADH) or SIADH has been reported in various disorders. We report a pediatric patient with nasopharynx carcinoma who may have developed a clinical SIADH with severe hyponatremia and generalized seizure during the administration of intravenous hydration. We propose that the inappropriately high plasma level of ADH led to the inability to excrete sufficient amounts of free water during a hyperhydration protocol with a relatively hypotonic fluid, which resulted in acute hyponatremia and central nervous system involvement. To avoid this complication, intravenous hydration before chemotherapy in children with nasopharynx carcinoma should be performed at a slower infusion rate and with a sodium chloride concentration of more than half isotonic.
Sujet(s)
Syndrome de sécrétion inappropriée d'ADH/étiologie , Tumeurs du rhinopharynx/complications , Enfant , Humains , MâleRÉSUMÉ
We report a case of bilateral abducens palsy as initial finding in nasopharyngeal carcinoma. Possible mode of involvement is discussed. Only one case has been reported in the past.
Sujet(s)
Nerf abducens , Carcinome épidermoïde/complications , Tumeurs du rhinopharynx/complications , Paralysie/étiologie , Carcinome épidermoïde/anatomopathologie , Atteintes des nerfs crâniens/complications , Atteintes des nerfs crâniens/diagnostic , Humains , Mâle , Adulte d'âge moyen , Tumeurs du rhinopharynx/diagnostic , Tumeurs du rhinopharynx/anatomopathologie , Paralysie/diagnosticRÉSUMÉ
Apresentamos um caso de paralisia bilateral do abducente como achado inicial em carcinoma de nasofaringe. Discute-se o modo de envolvimento. Somente um caso semelhante foi registrado anteriormente na literatura
Sujet(s)
Adulte d'âge moyen , Humains , Mâle , Nerf abducens , Carcinome épidermoïde/complications , Tumeurs du rhinopharynx/complications , Paralysie/étiologie , Carcinome épidermoïde/anatomopathologie , Atteintes des nerfs crâniens/complications , Atteintes des nerfs crâniens/diagnostic , Tumeurs du rhinopharynx/diagnostic , Tumeurs du rhinopharynx/anatomopathologie , Paralysie/diagnosticRÉSUMÉ
The angiofibroma of the nasopharynx is a benign tumor, sitting in the epipharynx of adolescents, but considered malignant owing to its local spreading power. Aside from the characteristics symptoms -nose bleeding and nasal obstruction- the A. of the paper has signaled a certain delay in the secondary sexual maturity of 2 of the 6 youth in all studied. In these 2 the tumor was detected at 9 and 12 years-of-age, respectively. Furthermore, these 2, showed destruction of inner structures of the nose when surgery was undertaken; adversely the other 4 showed normal inner nasal structures. The whole group was followed up for ten years, and only those 2 needed a treatment with chorionic gonadotrophin for the completeness of secondary sexual aspects.
Sujet(s)
Histiocytome fibreux bénin/complications , Muqueuse nasale/physiologie , Tumeurs du rhinopharynx/complications , Retard pubertaire/étiologie , Adolescent , Adulte , Enfant , Gonadotrophine chorionique/usage thérapeutique , Humains , Mâle , Tumeurs des sinus maxillaires/complications , Retard pubertaire/traitement médicamenteux , Caractères sexuelsRÉSUMÉ
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