Results 81 to 90 of about 6,751 (224)

Chinese Guidelines for Diagnosis and Treatment of Chronic Rhinosinusitis (2024)

World Journal of Otorhinolaryngology - Head and Neck Surgery, Volume 12, Issue 1, Page 25-55, February 2026.
ABSTRACT Chronic rhinosinusitis (CRS), a complex inflammatory disease with heterogeneous pathogenesis, demands evolving evidence‐based strategies. Since the 2018 Chinese guidelines and EPOS2020, international advances in CRS immunopathology and biologics have revolutionized therapeutic approaches, particularly through phenotype–endotype classification ...
Subspecialty Group of Rhinology, Editorial Board of Chinese Journal of Otorhinolaryngology Head and Neck Surgery, Subspecialty Group of Rhinology, Society of Otorhinolaryngology Head and Neck Surgery, Chinese Medical Association   +4 more
wiley   +1 more source

Lipoma of the Buccal Fat Pad: Systematic Review and Report of a Case

Oral Surgery, Volume 19, Issue 1, Page 57-67, February 2026.
ABSTRACT Introduction Lipomas in the oral cavity are uncommon, defined by the abnormal proliferation of mature adipocytes. When they arise from the buccal fat pad (BFP), these lipomas frequently impact both the cosmetic appearance and the functional aspects of the face. Objectives The aim of the present review is to investigate the incidence of the BFP
Silvia D'Agostino, Giulia Valentini, Marco Dolci   +2 more
wiley   +1 more source

A Topical Combination of 0.1 % Rapamycin And 0.1 % Tacrolimus Ointment for the Treatment of Facial Angiofibromas in Tuberous Sclerosis Complex – A Pilot Study of 5 Cases

Nepal Journal of Dermatology, Venereology & Leprology
Background: Facial angiofibroma represents the most conspicuous and cosmetic disfiguring cutaneous manifestation of tuberous sclerosis, frequently leading to stigma for both the affected individuals and their families. Many times these angiofibromas are
Ashish Jagati, Jeta Buch, Arpana Viradia, Bhargav Deshmukh, Sagar Chauhan, Santosh Dev Rothod   +5 more
doaj   +1 more source

Renal Angiomyolipoma in a Young Woman With Tuberous Sclerosis: A Case Report

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Tuberous sclerosis is a rare autosomal dominant genetic disorder caused by mutations in tumor suppressor genes (TSC1/2), leading to hamartomas in multiple organs. Renal angiomyolipomas are often asymptomatic but can cause mass effects or bleeding if they enlarge, requiring treatment.
Donald Dominick Lema, Bartholomeo Nicholaus Ngowi, Esther Lekei, Deardiana Sengelela, Furaha Kasyupa, Jeremia Pyuza, Denis Mucunguzi, Alex Mremi   +7 more
wiley   +1 more source

Endoscopic resection of nasopharyngeal angiofibroma: the role of radio-frequency coblation

Surgical Techniques Development, 2011
Nasopharyngeal angiofibromas are histologically benign but locally aggressive vascular tumors that can result in major morbidity and mortality. They exclusively affect adolescent male and are rare in patients older than 25 years.
Rohana Ali, Ivan Keogh, John Lang
doaj   +1 more source

British Association of Dermatologists and British Photodermatology Group guidelines for topical photodynamic therapy 2018 [PDF]

, 2019
The overall objective of the guideline is to provide up-to-date, evidence-based recommendations for the use of topical photodynamic therapy (PDT). The document aims to: • offer an appraisal of all relevant literature up to April 2018, focusing on any key
Collier, Nick, Exton, Luke S., Haylett, Ann K., Ibbotson, Sally, Mallipeddi, Rajeev, McKenna, K. E., Mohd Mustapa, M. Firouz, Morton, C. A., Moseley, Harry, Rhodes, Lesley E., Seukeran, Daron C., Ward, K. A., Wong, Terence   +12 more
core   +2 more sources

A rare form of discoid lupus erythematosus as a rosacea and angiofibroma: A case report

Clinical Case Reports, 2020
The rare presentation of DLE can be rosacea‐/angiofibroma‐like lesions which should be considered in patients with red‐pink to skin‐color papules with flushing and photosensitivity.
Fatemeh Mokhtari, Zakiye Ganjei
doaj   +1 more source

A late diagnose of malformation of ear tube: case report and review of literature [PDF]

, 2003
The malformation of the ear tube is a rare condition, usually diagnosed in children with recurrent otitis or deafness. There are no reports available in the medical literature attempting to this congenital malformation in older patients.
Alvarenga, Eliézia H. L., Cruz, Oswaldo Laércio Mendonça, Maia, Fabiana N. R., Souza, Márcia A.   +3 more
core   +5 more sources

Extranasopharyngeal Angiofibroma: A Diagnostic Dilemma

Philippine Journal of Otolaryngology Head and Neck Surgery, 2018
Objective: To report two cases of extranasopharyngeal angiofibroma, highlighting the diagnostic challenges involved. Methods:             Design:           Case Report             Setting:           Tertiary Teaching Hospital and Medical School
Nitin Gupta, Arjun Dass, Vaibhav Saini, Shashikant Anil Pol, Lovekesh Mittal   +4 more
doaj   +1 more source

Intensity modulated radiotherapy (IMRT) in the treatment of children and Adolescents - a single institution's experience and a review of the literature [PDF]

, 2009
Background While IMRT is widely used in treating complex oncological cases in adults, it is not commonly used in pediatric radiation oncology for a variety of reasons. This report evaluates our 9 year experience using stereotactic-guided, inverse planned
Florian Sterzing, Eva M Stoiber, Simeon Nill, Harald Bauer, Peter Huber, Jürgen Debus, Marc W Münter, Intensity Modulated Radiation Therapy Collaborative Working Group, A Eisbruch, C Nutting, A Pirzkall, W Zhen, MW Munter, D Schulz-Ertner, MW Munter, SL Wolden, G Studer, ML Cavey, M Guckenberger, L Veldeman, F Sterzing, A Boyer, TR Mackie, EJ Hall, EJ Hall, SF Kry, U Schneider, M Mazonakis, B Rhein, A Bhatnagar, JA Penagaricano, AC Paulino, BS Teh, JA Penagaricano, E Huang, N Jain, MJ Krasin, TM Schroeder, MW McDonald, AE Curtis, SE Combs, S Laskar, RB Kuppersmith, M Fuss, D Verellen, M Koshy, JS Welsh, EJ Hall, J Blatt, DG Gold, AC Paulino, HM Lin, LL Robison, GT Armstrong, F Nguyen, W Dorr, W Parker, A Rembielak   +57 more
core   +1 more source