Results 41 to 50 of about 729 (170)
Comparison of outcomes for balloon dilation of the Eustachian tube under local vs general anesthesia
Abstract Objective To compare the effectiveness of balloon dilation of the Eustachian tube (BDET) under local versus general anesthesia in the treatment of obstructive Eustachian tube dysfunction (OETD). Study Design Retrospective review. Methods Consecutive patients ages ≥18 with persistent OETD having failed adequate medical therapy underwent BDET ...
Joonas Toivonen +3 more
wiley +1 more source
Touraine-Solente-Gole Syndrome: A Rare Case Report
Touraine-Solente-Gole Syndrome, also known as Pachydermoperiostosis (PDP) or Primary Hypertrophic Osteoarthropathy, is a rare hereditary disorder, which affects both bones and skin.
Dharmil Doshi +2 more
doaj +1 more source
Pachydermoperiostosis ('Touraine-Solente-Gole' Syndrome)
DOI: http://dx.doi.org/10.3126/njdvl.v11i1.7937 Nepal Journal of Dermatology, Venereology & Leprology Vol.11(1) 2013 pp.64 ...
R Sharma +3 more
doaj +3 more sources
A Rare Cause of Refractory Anaemia hidden between Folds
British Journal of Haematology, Volume 202, Issue 4, Page 712-712, August 2023.
Syna Hamani +3 more
wiley +1 more source
Pachydermoperiostosis combined with pyloric gland adenoma with foveolar-type adenoma. [PDF]
United European Gastroenterology Journal, Volume 12, Issue 1, Page 152-154, February 2024.
Long B, Jiang C, Zheng Q, Wan P.
europepmc +2 more sources
Coexistence of Touraine-Solente-Gole syndrome and type 1 neurofibromatosis: A case report
Pachydermoperiostosis is a rare syndrome that affects the skin and skeletal system. Mutations in the gene encoding hydroxyprostaglandin dehydrogenase (HPGD) are thought to play a role in disease etiopathogenesis.
Selma Korkmaz +5 more
doaj +1 more source
Pachydermoperiostosis and bladder cancer [PDF]
Pachydermoperiostosis or the Touraine-Soulente-Golé syndrome is a rare monogenetic disorder characterized by pachydermia, periostosis and digital clubbing accounts for approximately 3∼5% of all patients with hypertrophic osteoarthropathy.
Stasolla, Alessandro +2 more
core +1 more source
Drug induced myocardial infarction is a known entity with different forms of steroids linked to coronary artery disease (CAD) either through promoting its traditional risk factors, inducing coronary spasm, or by other unidentified mechanisms. Dexamethasone is known to promote an atherogenic and hypercoagulable state.
Mohamed Shokr +4 more
wiley +1 more source
Cutis Verticis Gyrata Differential Diagnosis: Clinical Case
Background. Cutis verticis gyrata is rare benign scalp disorder characterized by excessive skin and subcutaneous tissue proliferation and hypertrophy. Nowadays, there are three forms of this disease with various developmental mechanisms and associated ...
Tatiana S. Belysheva +7 more
doaj +1 more source
ABSTRACT Primary hypertrophic osteoarthropathy (Pachydermoperiostosis) is a rare, inherited genetic disorder of the skeleton and the skin, characterised by clubbing of the fingers, thickening of the skin especially of the face and forehead (pachydermia) and periostosis. Patients often present with pain and swelling of the knees and ankles.
Ahmed AbdulBari +3 more
wiley +1 more source

