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
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Pachydermoperiostosis mimicking acromegaly: A case report [PDF]
Indian 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
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Distinct features of three clinical subtypes in 533 patients with primary hypertrophic osteoarthropathy [PDF]
Orphanet Journal of Rare DiseasesBackground Primary hypertrophic osteoarthropathy (PHO) is a rare genetic disorder classified into clinical subtypes and genetic subtypes. Previous clinical studies have primarily focused on case reports and family analyses, largely characterizing the ...
Xilei Cai +9 more
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Ayurveda management of Touraine–Solente–Gole syndrome: A clinical experience
Journal of Ayurveda Case ReportsTouraine–Solente–Gole syndrome, also known as pachydermoperiostosis (PDP) or primary osteoarthropathy, is a rare genetic disorder characterized by a distinctive triad: pachydermia (skin thickening), digital clubbing, and periostosis (excessive bone ...
T. Shrilatha Kamath, Anchumol Joseph
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Touraine-Solente-Gole syndrome with acne vulgaris successfully treated with isotretinoin [PDF]
Journal of Dermatology & Cosmetology, 2018 Touraine Solente Gole syndrome or pachydermoperiostosis is a rare genodermatosis affecting skin bones and connective tissue characterized by the triad of pachydermia periostosis and digital clubbing The authors report the case of a year old man presenting the dermato rheumatic symptoms that characterize the complete form of the syndrome He also ...
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Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report. [PDF]
Clin Case Rep, 2023 X‐ray of hand showing cortical thickening and periosteal reaction in distal radius ulna and phalynges of hand of a patient with pachydermoperiostosis. Key Clinical Message Pachydermoperiostosis is a rare genetic disorder that closely resembles acromegaly. Diagnosis is usually based on distinct clinical and radiological features. Oral etoricoxib therapy
Baniya A +6 more
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Frontal lifting using a tissue expander in pachydermoperiostosis: A case report. [PDF]
Clin Case Rep, 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 the rhytids prior to frontal lifting. The results were maintained after one year.
Cunha DJD +4 more
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Touraine-Solente-Gole Syndrome- A Rare Cause of Familial Periostosis
Journal of Evolution of Medical and Dental Sciences, 2020 Ajay Sharawat +3 more
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Touraine Solente Gole Syndrome (Pachydermoperiostosis): Case Report and Brief Review
Journal of the Turkish Academy of Dermatology, 2020 Zulfuqar Hasan Farajev +5 more
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Complete form of pachydermoperiostosis in a 16-year-old boy: A case report
Indian Journal of Paediatric Dermatology, 2022 Pachydermoperiostosis is an inherited osseocutaneous disorder. The unusual increased levels of prostaglandin E2 due to mutations in either HPGD gene or SLCO2A1 gene are regarded as the causative factor.
Sahana M Srinivas +3 more
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