Results 31 to 40 of about 6,672 (205)

Sirolimus Ointment for Facial Angiofibromas in Individuals with Tuberous Sclerosis Complex. [PDF]

open access: yes, 2017
BACKGROUND: Facial angiofibromas affect most patients with tuberous sclerosis complex. They tend to progress, can cause recurrent bleeding and facial disfigurement, and have significant psychological effects. We reviewed the effectiveness and safety of
Amin, S, Khan, A, Lux, A, O'Callaghan, F
core   +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

A case of inguinal cellular angiofibroma

open access: yesIJU Case Reports, 2020
Introduction Cellular angiofibroma is a benign mesenchymal tumor that is rare and has a good prognosis. However, preoperative distinction of cellular angiofibroma from malignant tumors is difficult.
Rei Kamitani   +7 more
doaj   +1 more source

Polypoidal Lesions in the Nasal Cavity [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2013
Introduction: Nasal polyps are polypoidal masses arising from mucous membranes of nose and paranasal sinuses. They are overgrowths of the mucosa that frequently accompany allergic rhinitis. They are freely movable and nontender.
Kalpana Kumari M.K., Mahadeva K.C.
doaj   +1 more source

Beyond the “3 Ps”: A critical appraisal of the non-endocrine manifestations of multiple endocrine neoplasia type 1

open access: yesFrontiers in Endocrinology, 2022
Multiple endocrine neoplasia type 1 (MEN1), an autosomal-dominantly inherited tumor syndrome, is classically defined by tumors arising from the “3 Ps”: Parathyroids, Pituitary, and the endocrine Pancreas.
Steven G. Waguespack
doaj   +1 more source

Primary Cardiac Angiofibroma [PDF]

open access: yesKorean Circulation Journal, 2013
Cardiac Angiofibroma is an uncommon intracardiac tumor. Thus far, only 4 cases of the rare intracardiac tumor have been reported. The present case-report describes an intracardiac angiofibroma in a 57-year-old healthy female. The patient was incidentally diagnosed with a left ventricle mass during echocardiography.
Kim, Young Ju   +4 more
openaire   +2 more sources

Retroperitoneal Cellular Angiofibroma: A Rare Gynecological Entity

open access: yesActa Médica Portuguesa, 2017
Cellular angiofibroma is a mesenchymal tumor, described in 1997, without gender preference, that usually appears at age 40. The vulvovaginal area is the most common site in women, mimicking vulvar benign tumors, like Bartholin gland cyst.
Ana Brandão   +4 more
doaj   +1 more source

A Giant Vulvar Mass: A Case Study of Cellular Angiofibroma

open access: yesCase Reports in Obstetrics and Gynecology, 2016
Cellular angiofibroma is a mesenchymal tumor that affects both genders. Nucci et al. first described it in 1997. Cellular angiofibroma is generally a small and asymptomatic mass that primarily arises in the vulvar-vaginal region, although rare cases have
Ümit Aydın   +4 more
doaj   +1 more source

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

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

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