Results 51 to 60 of about 5,241 (204)
Pre-auricular Subtemporal Approach for Intracranial Angiofibroma [PDF]
Iranian Journal of OtorhinolaryngologyIntroduction: 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
Indian 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
Frontiers 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
Clinical Case Reports, Volume 14, Issue 9, September 2026.ABSTRACT Tuberous sclerosis complex (TSC) is a rare multisystem genetic disorder characterized by the development of hamartomatous lesions in multiple organs. Although neurologic and dermatologic manifestations commonly lead to diagnosis during childhood, some patients remain undiagnosed until adulthood because of atypical presentations.
Kidus Tesfaye Bezabih +8 more
wiley +1 more source
Angiofibroma of the Nose [PDF]
The American Journal of the Medical Sciences, 1903 n ...
openaire +2 more sources
Endoscopic excision of Angiofibroma [PDF]
Indian 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
Clinical Case Reports, Volume 14, Issue 9, September 2026.ABSTRACT Retinal astrocytichamartoma (RAH) is a rare benign glial neoplasm most commonly associated with tuberous sclerosis complex (TSC). Sporadic cases, occurring in the absence of systemic phakomatosis, are uncommon and may closely mimic retinoblastoma, particularly when presenting with a calcified intraocular mass, creating a diagnostic challenge ...
Mesfin Wubishet Gurmu +7 more
wiley +1 more source
Apollo Medicine, 2021 Tuberous sclerosis complex (TSC) is a rare multisystem neurocutaneous disorder associated with the growth of benign tumors in different organs such as the brain, lungs, kidneys, heart, and eyes.
Aimen Malik +3 more
doaj +1 more source
Skin Research and Technology, Volume 32, Issue 9, September 2026.ABSTRACT Background Birt‐Hogg‐Dubé syndrome (BHDS) is a rare genetic tumor syndrome characterized by cutaneous fibrofolliculoma and trichodiscomas, lung bullae with an elevated risk of spontaneous pneumothorax and renal cell cancer. Objectives Due to rareness of the disease, clinical symptoms and cutaneous manifestations are often misjudged, resulting ...
Maximilian Deußing +7 more
wiley +1 more source
, 2017 RESUMEN Se realizó una breve revisión sobre los Angiofibromas Juveniles, presentándose un caso que acude al centro y es atendido en consulta externa por presentar epistaxis de moderada intensidad y una marcada obstrucción nasal.; en estudios ...
Raquel M García Alemán +5 more
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