Results 11 to 20 of about 740 (177)

Pachydermoperiostosis: a rare mimicker of acromegaly [PDF]

open access: yesEndocrinology, Diabetes & Metabolism Case Reports, 2017
Pachydermoperiostosis is a very rare osteoarthrodermopathic disorder whose clinical and radiographic presentations may mimic those of acromegaly. In the evaluation of patients with acromegaloid appearances, pachydermoperiostosis should be considered as
Noor Rafhati Adyani Abdullah   +2 more
doaj   +3 more sources

Pachydermoperiostosis as a Rare Cause of Blepharoptosis

open access: yesTürk Oftalmoloji Dergisi, 2014
A 37-year-old male patient diagnosed with pachydermoperiostosis at another center came to our clinic to rectify his blepharoptosis. The physical examination of the patient revealed skeleton and skin symptoms typical for pachydermoperiostosis.
Özlem Yalçın Tök   +5 more
doaj   +2 more sources

Pachydermoperiostosis mimicking acromegaly: A case report

open access: yesIndian Dermatology Online Journal, 2018
Pachydermoperiostosis is a rare, hereditary disease commonly presenting with digital clubbing, pachyderma, and periosteal hypertrophy. Coarsening of facial features and spade-like enlargement of hands and feet may give rise to a diagnostic dilemma ...
Prerna   +3 more
doaj   +2 more sources

Pachydermoperiostosis in a patient with chronic hepatitis B virus infection referred as acromegaly: a case report

open access: yesJournal of Medical Case Reports, 2018
Background Primary hypertrophic osteoarthropathy also known as pachydermoperiostosis is a rare genetic disorder that has often been confused with acromegaly because of similar clinical features.
Yacoba Atiase   +6 more
doaj   +2 more sources

Hypertrophy of the feet and ankles presenting in primary hypertrophic osteoarthropathy or pachydermoperiostosis: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2012
Introduction Pachydermoperiostosis or primary hypertrophic osteoathropathy is a rare genetic disease with autosomal transmission. This disorder, which affects both bones and skin, is characterized by the association of dermatologic changes (pachydermia ...
Akrout Rim   +5 more
doaj   +2 more sources

Bilateral ptosis as a presenting feature of primary hypertrophic osteoarthropathy (pachydermoperiostosis): a case report

open access: yesReumatismo, 2014
Pachydermoperiostosis is a rare hereditary disorder, which affects both bones and skin. It is characterized by a combination of dermatologic changes (pachydermia or thickening of the skin) and rheumatologic manifestations (periostosis and finger clubbing)
S. El Aoud   +4 more
doaj   +2 more sources

Pachydermoperiostosis: a case report [PDF]

open access: yesОстеопороз и остеопатии, 2017
Pachydermoperiostosis (PHO) or primary hypertrophic osteoarthropathy is a rare genetic disease that typically begins during childhood or adolescence. It is characterized by digital clubbing, pachydermia and periosteal reaction and progresses gradually ...
Valentina A. Fursenko   +3 more
doaj   +2 more sources

Pachydermoperiostosis or primary hypertrophic osteoarthropathy: A rare clinicoradiologic case

open access: yesIndian Journal of Radiology and Imaging, 2009
Pachydermoperiostosis (PDP) or primary hypertrophic osteoarthropathy is a rare syndrome with diverse radiological and clinical features. Though the diagnosis can be made on the basis of the classic clinical and radiological features, it is often missed ...
Rajul Rastogi   +5 more
doaj   +2 more sources

Reverse frontal lifting: alternative for the treatment of pachydermoperiostosis [PDF]

open access: yesRevista Brasileira de Cirurgia Plástica, 2020
Introduction: Patient diagnosed with pachydermoperiostosis, presenting a strong cutaneous manifestation, making it impossible to correct the defect by the usual facial lifting techniques.
Ronaldo Pontes   +4 more
doaj   +3 more sources

Home - About - Disclaimer - Privacy