Results 51 to 60 of about 4,912 (206)

Central retinal artery occlusion following embolization in juvenile nasopharyngeal angiofibroma: A case report [PDF]

open access: yesVojnosanitetski Pregled, 2018
Introduction. Juvenile nasopharyngeal angiofibromas are highly vascular, locally aggressive lesions, that affect male adolescents. The surgery is the treatment of choice, although it shows a strong propensity to bleed during surgical removal ...
Pantelić Jelica   +3 more
doaj   +1 more source

Angiofibroma of the Nose [PDF]

open access: yesThe American Journal of the Medical Sciences, 1903
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openaire   +2 more sources

Parotid angiofibroma

open access: yesJournal of Oral and Maxillofacial Pathology, 2014
Angiofibromas are rare, benign, locally invasive vascular tumors, which represent 0.05-0.5% of all head and neck tumors. Most frequent site of occurrence is the posterior nasopharynx, called as nasopharyngeal angiofibromas (NA), when these arise outside the nasopharyngeal region they are termed as extranasopharyngeal angiofibromas (ENA).
Hallur, Neelakamal H   +3 more
openaire   +3 more sources

Pre-auricular Subtemporal Approach for Intracranial Angiofibroma [PDF]

open access: yesIranian Journal of Otorhinolaryngology
Introduction: In around 10-20% of angiofibroma cases, the tumor penetrates the skull base to involve intracranial structures, posing difficulty in treating them surgically. Today, advancement in skull base surgery has brought about a paradigm shift, and
Neizekhotuo Shunyu   +4 more
doaj   +1 more source

Cutaneous angiofibroma: A clinching evidence for diagnostic workup of tuberous sclerosis complex

open access: yesIndian Journal of Dermatopathology and Diagnostic Dermatology, 2020
Tuberous sclerosis complex (TSC) or Bourneville's disease is a genetic multisystem disorder of multisite hamartomas. Majority of TSC cases are sporadic.
Bhushan M Warpe   +3 more
doaj   +1 more source

Cutaneous lesions and other non-endocrine manifestations of Multiple Endocrine Neoplasia type 1 syndrome

open access: yesFrontiers in Endocrinology, 2023
BackgroundMultiple Endocrine Neoplasia type 1 is a rare genetic syndrome mainly caused by mutations of MEN1 gene and characterized by a combination of several endocrine and non-endocrine manifestations.
Laura Pierotti   +12 more
doaj   +1 more source

Endoscopic excision of Angiofibroma [PDF]

open access: yesIndian Journal of Otolaryngology and Head & Neck Surgery, 2001
We present a case of Juvenile Nasopharyngeal Angiofibroma (JNA) managed by endoscopic excision alone. The selection of the case, technical difficulties and the advantages offered by this technique are detailed.
R, Bradoo   +3 more
openaire   +2 more sources

The Natural History of Residual and Recurrent Disease in Advanced Juvenile Nasopharyngeal Angiofibroma: A Systematic Review

open access: yesThe Laryngoscope, EarlyView.
Residual and recurrent disease in advanced juvenile nasopharyngeal angiofibromas (JNAs) demonstrate spontaneous involution, reduction in size, or long‐term stability following initial treatment in 95% of patients. In this systematic review of 131 patients with advanced JNA, only 2% of patients demonstrated disease progression during surveillance, but ...
Shivani Angelique Kumar   +2 more
wiley   +1 more source

Applications and prospects of artificial intelligence and digital medicine in pediatric nasal skull base tumors

open access: yesPediatric Investigation, EarlyView.
Pediatric nasal skull base tumors present diagnostic and therapeutic challenges due to their deep location, nonspecific symptoms, and the narrow nasal cavity in children. Although artificial intelligence (AI) and digital medicine have advanced early diagnosis, multidisciplinary treatment, and prognosis, their application in these rare tumors remains ...
Xiuping Wu   +5 more
wiley   +1 more source

Endoscopic Surgery of Juvenile Angiofibroma

open access: yes, 2017
Surgery is considered the gold standard for the treatment of juvenile angiofibroma (JA), and preoperative embolization has provided significant reduction of complications and intraoperative bleeding with minimal risk of residual disease.
A Safadi   +5 more
core   +1 more source

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