ArticleAnais brasileiros de dermatologia
Complete form of pachydermoperiostosis.
Article in Anais brasileiros de dermatologia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 18 citations in OpenAlex.
- Pachydermoperiostosis Associated With a Rare SLCO2A1 Mutation: A Case Report and Literature Review.Cureus · 2025Article
- Familial complete pachydermoperiostosis presenting with vertebral hypertrophy and myelopathy.JBMR plus · 2025Article
- Distinct features of three clinical subtypes in 533 patients with primary hypertrophic osteoarthropathy.Orphanet journal of rare diseases · 2025Article
- Primary hypertrophic osteoarthropathy: phenotypic variability and penetrance rate in heterozygotes forJBMR plus · 2025Article
- Pachydermoperiostosis Due to a NovelJCEM case reports · 2024Article
- Clinical Outcomes of Utilizing a "W"-shaped Incision in the Management of Forehead Skin Thickening Induced by Hypertrophic Osteoarthropathy.Aesthetic plastic surgery · 2024Article
- Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report.Clinical case reports · 2023Article
- Touraine-Solente-Gole syndrome: pathogenic variant in SLCO2A1 presented with polyarthralgia and digital clubbing.Pediatric rheumatology online journal · 2023Article
- A Complete Form of Pachydermoperiostosis Accompanied by a Pituitary Microadenoma.Clinical, cosmetic and investigational dermatology · 2023Article
- A Case of Progressive Thickening and Furrowing of Facial Skin and Scalp with Scarring Alopecia.Skin appendage disorders · 2021Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
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 data. A complete form of the syndrome is reported in a male patient with disease onset in adolescence, with compatible clinical and radiological findings, presenting the three cardinal findings as well as other associated manifestations, such as hyperhidrosis and acne.
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