Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report [PDF]
Clinical 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.
Abinash Baniya, Manoj Shahi
exaly +4 more sources
A case report of an extremely rare association of ankylosing spondylitis with pachydermoperiostosis [PDF]
Clinical 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 +3 more sources
A Complete Form of Pachydermoperiostosis Accompanied by a Pituitary Microadenoma [PDF]
Clinical, 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,
Yanjing Chen
exaly +4 more sources
Comprehensive Treatment of a Rare Case of Complete Primary Pachydermoperiostosis with Large Facial Keloid Scars: A Case Report and Literature Review [PDF]
Case Reports in DermatologyIntroduction: 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 +5 more sources
Pachydermoperiostosis Mimicking Inflammatory Arthritis: Case Description and Narrative Review [PDF]
Rheumato, 2023 Pachydermoperiostosis (PDP), also called primary hypertrophic osteoarthropathy (HOA), is a rare genetic disease with typical thickening of the skin (pachydermia) and rheumatic manifestations, with clubbing of the fingers and toes and periostosis of the ...
AKM Kamruzzaman +7 more
doaj +3 more sources
Pachydermoperiostosis: a rare mimicker of acromegaly [PDF]
Endocrinology, 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
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Differential Diagnosis of Acromegaly: Pachydermoperiostosis Two New Cases from Turkey [PDF]
JCRPE, 2022 Pachydermoperiostosis (PDP), also known as primary hypertrophic osteoarthropathy, is a rare genetic disorder characterized by pachyderma and periostosis.
Emine Kartal Baykan, Ayberk Türkyılmaz
doaj +2 more sources
A patient with pachydermoperiostosis harboring SLCO2A1 variants with a history of differentiating from acromegaly [PDF]
Bone 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 +2 more sources
Frontal lifting using a tissue expander in pachydermoperiostosis: A case report [PDF]
Clinical 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: Three Case Reports
Journal 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