Results 31 to 40 of about 635 (170)
Complete form of pachydermoperiostosis, [PDF]
Anais Brasileiros de Dermatologia, 2020 Pachydermoperiostosis (PDP) or primary hypertrophic osteoarthropathy (PHO) is a rare hereditary disease characterized by digital clubbing, pachydermia, and periostosis. Its pathogenesis is uncertain and the diagnosis is based on clinical and radiological
Mônica Larissa Padilha Honório +2 more
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Bilateral Ptosis Due to a Rare Cause-Pachydermoperiostosis [PDF]
Journal of Clinical and Diagnostic Research, 2013 Pachydermoperiostosis is a rare hereditary disorder that is characterised by pachydermia (thickening of the facial skin and/ or scalp), and periostosis (swelling of the periarticular tissue and a subperiosteal new bone formation).
Mahesh M, K V K S N Murthy
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Etiology of pachydermia diffusa. Proposal of a hypothesis and afterward development.
Japanese Journal of Clinical Immunology, 1997 Kazuhiko Takehara
openalex +3 more sources
Endoscopic approach to hyperplastic laryngeal lesions: a literature review and personal experience
The Egyptian Journal of Otolaryngology, 2023 Background Presently, there is a lot of confusion in the identification and classification and no consensus regarding the management of hyperplastic laryngeal lesions (HLL).
Petru Gurău
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Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report
Clinical Case Reports, Volume 11, Issue 6, June 2023., 2023 X‐ray of hand showing cortical thickening and periosteal reaction in distal radius ulna and phalynges of hand of a patient with pachydermoperiostosis. Key Clinical Message Pachydermoperiostosis is a rare genetic disorder that closely resembles acromegaly. Diagnosis is usually based on distinct clinical and radiological features. Oral etoricoxib therapy
Abinash Baniya +6 more
wiley +1 more source
Cutis verticis gyrata in a 24‐year‐old young man revealing a T‐cell lymphoblastic lymphoma
Clinical Case Reports, Volume 10, Issue 10, October 2022., 2022 Abstract T‐cell lymphoblastic lymphoma (T‐LBL) is frequently revealed by amediastinal mass or peripheral lymphadenopathy. Skin lesions in T‐LBLusually present as multiple nodules associated with multiple peripherallymphadenopathy and bone marrow invasion. Our patient is particular bythe revealing presentation of the lesions as Cutis verticis gyrate.
Sarra Saad +6 more
wiley +1 more source
Comparison of outcomes for balloon dilation of the Eustachian tube under local vs general anesthesia
Laryngoscope Investigative Otolaryngology, Volume 7, Issue 4, Page 1120-1128, August 2022., 2022 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
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Pachydermoperiostosis ('Touraine-Solente-Gole' Syndrome)
Nepal Journal of Dermatology, Venereology & Leprology, 2013 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
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A Rare Cause of Refractory Anaemia hidden between Folds
, 2023 British Journal of Haematology, Volume 202, Issue 4, Page 712-712, August 2023.
Syna Hamani +3 more
wiley +1 more source
Touraine-Solente-Gole Syndrome: A Rare Case Report
Delhi Journal of Ophthalmology, 2017 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
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