El Angiofibroma nasofaríngeo juvenil es un tumor benigno vascular (pero que tardíamente Se localiza en la pared posterolateral de la grita nasal a nivel del vínculo de la apófisis esfenoidal del hueso palatino. Esta localización conforma el. Nasal cavity, paranasal sinuses, nasopharynx – Nasopharyngeal angiofibroma. Juvenile nasopharyngeal angiofibroma (JNA) is a rare and benign but locally in the nasopharynx and nasal cavity, leading to manifestations such as nasal.
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Strayer; Emanuel Rubin Type III is a calabash-like massive tumor lobe in the middle cranial fossa. Health care resources for this disease Expert centres Diagnostic tests 1 Patient organisations 24 Orphan drug s 1. Sarcoma Lymphoma Immature teratoma Melanoma. Intracranial intradural tumor without infiltration of the cavernous sinus, pituitary fossa or optic chiasm. Sign up for our Email Newsletters. The location and size of the tumor and feeding vessels are clearly demonstrated by this technique.
Juvenile nasopharyngeal angiofibroma
J Clin Imaging Sci. The demographic profile, surgical techniques ansal, immediate and delayed complications, and recurrence rate of the sample are listed in Table 1. A case report of JNA with rare intra-oral manifestation in a year-old male patient is presented in the article. Detailed information Article for general public English Discussion Juvenile nasopharyngeal angiofibromas present almost exclusively in men aged years A concise classification system and appropriate treatment options.
jucenil Although it is a rare neoplasm, accounting for less than 0. Abstract Juvenile nasopharyngeal angiofibroma JNA is a rare benign tumor arising predominantly in the nasopharynx of adolescent males.
The presentation is typically with obstructive symptoms, epistaxisand chronic otomastoiditis due to obstruction of the Eustachian tube. Findings are similar to those described above.
Angiofibroma nasofaríngeo juvenil – Wikipedia, la enciclopedia libre
The presence of prominent flow voids lead to a salt and pepper appearance on most sequences and are characteristic 5,6. Intracranial extension, residual vascularity; M: The authors believe that this injury may have been secondary to the heat of electrocoagulation.
Endoscopic surgery was performed in three patients, without postoperative complications; endoscopic-assisted surgery in three others, with two instances of complications, and external surgery in seven.
Sanchez de Guzman G. W B Saunders Co.
Other essential requirements for the endoscopic approach include adequate surgeon experience, availability of proper instruments, performance of preoperative embolization, and the possibility of adding an open route if necessary. Mast cells and T-lymphocytes in juvenile angiofibromas. For treatment of small lesions, external surgical approaches are gradually being replaced by endoscopic surgery, which can also be combined with conventional approaches in cases basal more advanced disease. Juvenile nasopharyngeal angiofibroma JNA is a benign neoplasm of the nasopharynx.
Impaired Eustachian tube function, facial deformity, proptosis and changes in visual acuity may be seen. Endoscopic surgery for juvenile nasopharyngeal angiofibroma: JNA is an uncommon, highly vascular, locally invasive, unencapsulated tumor with a distinct predilection for an origin in the nasopharynx of adolescent males.
The disease-free period ranged from 10 to 36 months postoperatively. Recent advances in the treatment of juvenile angiofibroma. Analysis of these 13 patients suggests that naal endoscopic surgery is viable angiofibrmoa in advanced cases of JNA. Conclusion Nasal endoscopy, alone or combined with open juvenio, was safe for the resection of angiofibromas at different stages, with low morbidity and high efficacy, as shown by complete tumor removal and low recurrence rates.
Oronasal fistula a possible complication of preoperative embolization in the management of juvenile nasopharyngeal angiofibroma. Figure 7 shows mast cells in toluidine blue stain. The first patient who underwent surgery in our department had a Fisch I tumor, but did juveni undergo embolization or clamping of the external carotid arteries. Overlying mucosa appeared normal.
The volume of intraoperative bleeding has been shown to be similar in patients with and without embolization 34whereas tendency to relapse was greater in patients undergoing embolization. In both cases, jvuenil combined surgical approach had been employed. Mean patient age was Provisional diagnosis of nasopharyngeal angiofibroma, soft tissue tumor, nasopharyngeal polyp or vascular tumor was made.
Juvenile nasopharyngeal angiofibroma
Factors analyzed include patient age and gender, symptoms, stages, treatment, length of surgery, intraoperatory bleeding, postoperative need for nasal tampons, hospitalization time, complications, and tumor recurrence. Molecular pathogenesis of juvenile nasopharyngeal angiofibroma in Brazilian patients.
juveinl The tumors are frequently located in the posterolateral angiofibrma of the nasal cavity, where the sphenoid process of the palatine bone articulates with the base of the pterygoid process, forming the sphenopalatine foramen. Intraoperative control of bleeding during the resection of nasopharyngeal angiofibromas can be achieved successfully by temporary clamping of the external carotid arteries in the neck However, as in any invasive procedure, embolization presents risks that should be fully explained to the patients