Results 1 to 10 of about 740 (177)

A case report of an extremely rare association of ankylosing spondylitis with pachydermoperiostosis [PDF]

open access: yesClinical Case Reports, 2023
Key Clinical Message We describe a case of a young man with features of pachydermoperiostosis and spondyloarthropathy. By describing this rarity, we aim to help build a database for future studies and construct a management plan that rheumatologists and ...
Faiq I. Gorial   +2 more
doaj   +4 more sources

Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report [PDF]

open access: yesClinical Case Reports (discontinued), 2023
Key Clinical Message Pachydermoperiostosis is a rare genetic disorder that closely resembles acromegaly. Diagnosis is usually based on distinct clinical and radiological features.
Manoj Shahi, Abinash Baniya
exaly   +4 more sources

A Complete Form of Pachydermoperiostosis Accompanied by a Pituitary Microadenoma [PDF]

open access: yesClinical, Cosmetic and Investigational Dermatology, 2023
Yan Jing Chen, Li Li Department of Dermatology and Venereology, West China Hospital, Sichuan University, Chengdu, Sichuan, People’s Republic of ChinaCorrespondence: Li Li, Department of dermatology and venereology, West China Hospital, Sichuan University,
Chen YJ, Li L
exaly   +4 more sources

A patient with pachydermoperiostosis harboring SLCO2A1 variants with a history of differentiating from acromegaly [PDF]

open access: yesBone Reports, 2023
Pachydermoperiostosis (PDP) is a rare hereditary disease characterized by digital clubbing, pachydermia, and periostosis. We describe a Japanese male patient with PDP who was differentially diagnosed with acromegaly by identification of compound ...
Yukako Nakano   +5 more
doaj   +3 more sources

Complete form of pachydermoperiostosis, [PDF]

open access: yesAnais 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
doaj   +3 more sources

Cutis Verticis Gyrata Across the Diagnostic Spectrum: Two Cases Highlighting Challenges in Clinical Classification [PDF]

open access: yesClinical Case Reports
Cutis verticis gyrata (CVG) is an uncommon disorder characterized by cerebriform thickening of the scalp that may occur as a primary condition or secondary to a variety of systemic disorders.
Sanket Bishokarma   +2 more
doaj   +2 more sources

Comprehensive Treatment of a Rare Case of Complete Primary Pachydermoperiostosis with Large Facial Keloid Scars: A Case Report and Literature Review [PDF]

open access: yesCase Reports in Dermatology
Introduction: Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy, is a rare autosomal dominant disease with primary clinical features of pachydermia (thickening of skin) and periostosis (new bone formation).
Haibo Zhao   +3 more
doaj   +2 more sources

Pachydermoperiostosis: Three Case Reports

open access: yesJournal of Orthopaedic Surgery, 2001
Three patients with pachydermoperiostosis are reported. All patients presented with moderate pain and swelling in multiple joints unresponsive to treatment, characteristic facial features which were marked in two cases, clubbing of nails and enlargement ...
Kumar Bhaskaranand   +2 more
exaly   +2 more sources

Frontal lifting using a tissue expander in pachydermoperiostosis: A case report [PDF]

open access: yesClinical Case Reports, 2021
Pachydermoperiostosis, a rare condition, is characterized by pachydermia, finger clubbing, and periostosis. We present an unusual treatment for frontal rhytids, for which we used a tissue expander that contributed to thinning of the skin and the depth of
Daniel José Dias Cunha   +4 more
doaj   +2 more sources

Pachydermoperiostosis [PDF]

open access: yesMedical Journal Armed Forces India, 2010
A G, Sasane   +3 more
exaly   +3 more sources

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