Results 1 to 10 of about 2,068 (238)

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

open access: goldClinical 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   +6 more sources

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

open access: yesClinical Case Reports, 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   +6 more
doaj   +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]

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   +6 more sources

Pachydermoperiostosis: a rare mimicker of acromegaly [PDF]

open access: goldEndocrinology, 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   +6 more sources

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

open access: goldClinical 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   +5 more sources

Pachydermoperiostosis Mimicking Inflammatory Arthritis: Case Description and Narrative Review [PDF]

open access: yesRheumato, 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   +4 more sources

Pachydermoperiostosis combined with pyloric gland adenoma with foveolar-type adenoma. [PDF]

open access: yesUnited European Gastroenterol J, 2023
United European Gastroenterology Journal, Volume 12, Issue 1, Page 152-154, February 2024.
Long B, Jiang C, Zheng Q, Wan P.
europepmc   +3 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
doaj   +3 more sources

Pachydermodactyly: An Underdiagnosed Condition in Adolescence—A Case Report and Literature Review [PDF]

open access: yesCase Reports in Dermatological Medicine
Pachydermodactyly (PDD) is a rare, underdiagnosed benign condition characterized by asymmetrical, bilateral fusiform swellings of the hands’ proximal interphalangeal (PIP) joints.
Mishari T. Alrubaiaan   +2 more
doaj   +3 more sources

Acetaminophen as a possible safer alternative for reducing prostaglandin E2‐major urinary metabolites concentrations and alleviating joint pain in pachydermoperiostosis

open access: yesJEADV Clinical Practice
JEADV Clinical Practice, Volume 4, Issue 1, Page 277-280, March 2025.
Tomoya Takegami   +13 more
doaj   +3 more sources

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