Results 151 to 160 of about 4,912 (206)

Tuberous sclerosis with recurrent seizure, dermatological lesions, renal cysts, and hypothyroidism in a female patient in Awka, Nigeria. [PDF]

Niger Med J
Anyabolu EN, Ufoaroh CU, Okoli OI, Izuu-Umeike AO.   +3 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Radiological findings in angiofibroma

Acta Radiologica, 2000
Surgery after pre-operative embolization has become the main treatment modality in angiofibroma therapy. As surgical planning is based on precise pre-operative tumour evaluation, knowledge of the characteristic growth patterns is of great interest. Analysis of tumour extension and blood supply, as well as methods of controlling intra-operative bleeding,
B, Schick, G, Kahle
exaly   +3 more sources

Cellular Angiofibroma of the Nasopharynx

Journal of Craniofacial Surgery, 2017
Abstract Angiofibroma is a common tumor of the nasopharynx region but cellular type is extremely rare in head and neck. A 13-year-old boy presented with frequent epistaxis and nasal obstruction persisting for 6 months. According to the clinical symptoms and imaging studies juvenile angiofibroma was suspected.
Erdur, Zulkuf Burak, Yener, Haydar Murat, Yilmaz, Mehmet, Karaaltin, Aysegul Batioglu, Inan, Hakki Caner, Alaskarov, Elvin, Gozen, Emine Deniz   +6 more
openaire   +3 more sources

Juvenile Nasopharyngeal Angiofibroma

Otolaryngologic Clinics of North America, 2011
Juvenile nasopharyngeal angiofibromas (JNAs) are rare, benign, highly vascular, locally aggressive tumors that primarily affect male adolescents. Historical treatment of these neoplasms has been primarily surgical. In the past decade, endoscopic resection of JNAs has become a viable and promising surgical treatment option. Endoscopic resection has many
Angela, Blount, Kristen O, Riley, Bradford A, Woodworth   +2 more
openaire   +3 more sources

The nasopharyngeal angiofibroma

International Journal of Radiation Oncology*Biology*Physics, 1977
Between 1948 and 1975, we have seen 48 patients with nasopharyngeal angiofibroma. Radiotherapy is the treatment of choice for most patients. A dose of 3,000 rads in three weeks leads to thrombosis, fibrosis, and tumor regression, although a latent period up to two years may elapse before final disappearance.
P J, Fitzpatrick, T D, Briant, J M, Berman   +2 more
openaire   +2 more sources

Angiofibroma of the Vulva

Journal of Cutaneous Medicine and Surgery, 2014
Background: Cellular angiofibroma is a benign and rare tumor. It usually arises in middle-aged women and involves the vulva. Complete local excision of the tumor is the best cure, and, usually, there is no recurrence after surgery. Case Report:
Hassan, Ahmadnia, Ali, Kamalati, Mahmood, Dolati, Alireza, Akhavan Rezayat, Mehrdad, Katebi   +4 more
openaire   +2 more sources

Extranasopharyngeal angiofibroma

International Journal of Pediatric Otorhinolaryngology, 2000
Juvenile nasopharyngeal angiofibromas are vascular neoplasms, which originate characteristically in the posterior lateral wall of the nasopharynx. Although angiofibromas extend beyond the nasopharynx commonly, they rarely originate outside the nasopharynx. Reports of primary extranasopharyngeal angiofibromas have appeared sporadically in the literature.
R Y, Huang, E J, Damrose, K E, Blackwell, A N, Cohen, T C, Calcaterra   +4 more
openaire   +2 more sources

Nasopharyngeal angiofibroma

The Journal of Laryngology & Otology, 1978
Three cases of nasopharyngeal angiofibroma have been described along with the histopathological findings, treatment and a brief review of the literature on the subject. It is of interest that one of these cases, histologically proven, was a female and this in spite of some rigidly held views about the strict sex linkage of the lesion.
F D, Martinson, I, Samuel
openaire   +2 more sources