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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Nasopharyngeal angiofibroma – Wikipedia

Arterial embolization in the management of posterior epistaxis. Changes in staging and treatment.

Minimal extension through the angiofibroka foramen, into and including a minimal part of the medial-most part of the pterygomaxillary fossa. All patients were treated surgically, muvenil 17 who underwent endoscopic surgery. Extended osteoplastic maxillotomy for total excision of giant multicompartmental juvenile nasopharyngeal angiofibroma. However, in view of the findings of this study, fully endoscopic or endoscopic-guided access should be considered even for advanced-stage tumors with major intracranial extension.

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 Evaluation of the effectiveness of preoperative embolization in surgery for nasopharyngeal angiofibroma. Service chief medical residency in Otorhinolaryngology, Universidade Federal de Sergipe.


Pathology Outlines – Nasopharyngeal angiofibroma

Arteriography followed by preoperative embolization and surgical resection is the treatment of choice. Angiofibroma; Endoscopy; Video-assisted surgery; Recurrence; Intraoperative complications; Postoperative complications.

This feature may be helpful is differentiating from other more aggressive lesions. Intracranial extension, residual vascularity; L: The classification and clinical staging is relatively easy and helps to plan treatment and determine prognosis.

These tumors occur almost exclusively in male adolescents and account for 0. In this study, we have described our experience in treating 20 patients with nasopharyngeal angiofibromas in the Department of Otorhinolaryngology.

Nasopharyngeal angiofibroma

Olfactory neuroblastoma Olfactory neuroblastoma. Results Thirteen patients met the criteria for inclusion and underwent surgical treatment.

For example, a retrospective study of 15 patients found tumor recurrence in 1 patient 6. From Wikipedia, the free encyclopedia. Thirteen patients underwent surgery. These lesions include inflammatory polyps, angiomatous polyps, nasopharyngeal cysts and carcinomas, soft tissue neoplasms such as papilloma, lymphoma, neurofibroma, maxillary malignancies, nasal fossa esthesioneuroblastoma, adenoid hypertrophy, cervical vertebrae cordomas and retropharyngeal ganglia tuberculosis.

Nasal cavity, paranasal sinuses, nasopharynx Other tumors Nasopharyngeal angiofibroma Author: In one patient, the procedure had to be halted due to persistent hypovolemic shock despite transfusion, and only partial resection of the tumor was achieved.

Complications in the endoscopic and endoscopic-assisted treatment of juvenile nasopharyngeal angiofibroma with intracranial extension. Extensive bony destruction is usually not a feature, angiiofibroma rather bone is remodelled or resorbed. Numerical sex chromosome aberrations in juvenile angiofibromas: Histopathologically JNA shows a fibrocellular stroma with angioffibroma cells and haphazardly arranged collagen interspersed with an irregular vascular pattern.


The other 17 patients required only endoscopic surgery. Genetic evidence for an androgen-dependent tumor? Log in Sign up.

Angiofibromas originating outside the nasopharynx may appear as an intraoral mass in the retromolar or buccal space area. The success rates and low intra- and postoperative complication rates of endoscopic surgery suggest that this route has been gaining ground in the management of Radkowski IIIa class JNAs. Publicado por Elsevier Editora Ltda. In jasal, Friedberg called it juvenile angiofibroma.

Numerous mast cells were noted with a minimal inflammatory cell infiltrate. Several reports suggest that JNA regresses over time. Recent advances in the treatment of juvenile angiofibroma. Juvenile nasopharyngeal angiofibroma is a rare, highly vascular, and histologically benign tumor, generally observed in male adolescents.