Results 181 to 190 of about 6,672 (205)
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Extranasopharyngeal juvenile angiofibroma

The Journal of Laryngology & Otology, 1975
A rare case of juvenile angiofibroma arising from the base of the skull outside the nasopharynx and extending into the pterygo-maxillary fossa and cheek is discribed. It is possible, by a combined zygomatic and buccal approach, successfully to excise such a tumour.
I, Isherwood   +2 more
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Juvenile nasopharyngeal angiofibroma

Oral Surgery, Oral Medicine, Oral Pathology, 1973
Abstract The juvenile nasopharyngeal angiofibroma is a histologically benign, clinically aggressive neoplasm arising primarily in the nasopharynx of adolescent males. Diagnosis and treatment often present difficulty. The potential for these tumors to involve the perioral structures requires that the clinician conducting an intraoral examination be ...
J L, Hicks, J F, Nelson
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Juvenile Nasopharyngeal Angiofibroma

Otolaryngologic Clinics of North America, 1986
JNA is a highly vascular, benign, yet locally invasive tumor that occurs in preadolescent males. Diagnosis is based on history, physical examination, and radiographic findings. CT scanning is invaluable for evaluating tumor extent. Angiography combined with embolization aids surgeons in identifying the main feeding vessels and decreasing intraoperative
V, Grybauskas, J, Parker, M, Friedman
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Juvenile Nasopharyngeal Angiofibroma

Otolaryngologic Clinics of North America, 1965
JUVENILE nasopharyngeal angiofibroma is an uncommon tumor found in the nasopharynx of the adolescent male. It is a highly vascular, locally invasive, nonencapsulated lesion which begins in the pubescent period and causes varying symptoms during the adolescent years.
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Extranasopharyngeal angiofibroma revisited

Clinical Otolaryngology, 2017
BackgroundAngiofibromas in the head and neck region usually arise in the nasopharynx, but may also occur elsewhere. This study aims at evaluating the incidence and clinical features of extranasopharyngeal angiofibroma (ENA).Material and MethodsSystematic review of the literature (Medline® and Google™) up to 31 December 2015.Results174 cases of ENA were
J.P. Windfuhr, J. Vent
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Juvenile Nasopharyngeal Angiofibroma

Archives of Pediatrics & Adolescent Medicine, 1981
• The pediatrician is often the first physician to see the patient afflicted with a nasopharyngeal angiofibroma. This benign but dangerous tumor is unique because of its exclusive affinity for male children, its consistent location in the posterior nares-nasopharyngeal area, and its tendency to invade the base of the skull in a significant percentage ...
R B, Sessions, D P, Zarin, R N, Bryan
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Juvenile nasopharyngeal angiofibroma

The Laryngoscope, 1972
AbstractThis paper contains a review of the gross pathology and histopathology of juvenile nasopharyngeal angiofibroma and a review of the theories of origin of this tumor. The relative merits of hormone therapy, carotid arteriography, external and interstitial radiation therapy, cryosurgery, and various surgical approaches are discussed.A plan for the
W R, Wilson   +3 more
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Juvenile Nasopharyngeal Angiofibroma

Annals of Otology, Rhinology & Laryngology, 1978
The diagnosis of angiofibroma can be suspected in most cases by clinical examination, supplemented by routine x-rays and tomograms and is confirmed by angiography. Adjunctive therapy including embolization, estrogens, cryotherapy and arterial ligation is discussed. Surgical resection is the preferred treatment.
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Paranasal Juvenile Angiofibroma

Archives of Otolaryngology - Head and Neck Surgery, 1962
The possibility of juvenile nasopharyngeal angiofibroma originating in areas other than the vault of the nasopharynx has long been recognized in the European literature, 1 but the English literature scarcely mentions extranasopharyngeal origin. In 1959 one of us (J.F.H.) encountered a tumor identical to a nasopharyngeal angiofibroma originating from ...
J F, HORA, A K, BROWN
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Juvenile nasopharyngeal angiofibroma

Journal of Surgical Oncology, 1980
AbstractSeven cases of juvenile nasopharyngeal angiofibroma were seen in the Division of Radiation Oncology of the Department of Human Oncology, University of Wisconsin Hospitals from 1961 to 1977. The method of treatments and the end results are discussed.
S P, Vadivel, A, Bosch, B, Jose
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