Primary hypertrophic osteoarthropathy: genetics, clinical features and management

Q Lu, Y Xu, Z Zhang, S Li, Z Zhang - Frontiers in Endocrinology, 2023 - frontiersin.org
Primary hypertrophic osteoarthropathy (PHO) is a genetic disorder mainly characterized by
clubbing fingers, pachydermia and periostosis. Mutations in the HPGD or SLCO2A1 gene …

Hypertrophic osteoarthropathy

M Martínez-Lavín - Best Practice & Research Clinical Rheumatology, 2020 - Elsevier
Hypertrophic osteoarthropathy (HOA) is an orphan syndrome characterized by abnormal
proliferation of the skin and osseous tissues at the distal parts of the extremities. The main …

[HTML][HTML] Safety and efficacy of cyclooxygenase-2 inhibition for treatment of primary hypertrophic osteoarthropathy: a single-arm intervention trial

L Yuan, R Liao, Y Lin, Y Jiang, O Wang, M Li… - Journal of orthopaedic …, 2019 - Elsevier
Background Primary hypertrophic osteoarthropathy (PHO) is a rare disease involving joint,
bone and skin. Two underlying genes responsible for this disease—hydroxyprostaglandin …

Role of bisphosphonates in hypertrophic osteoarthropathy: a systematic review

R Palui, K Sridharan, J Sahoo, V Suryadevara… - Endocrine, 2024 - Springer
Background The role of bisphosphonates (BP) in hypertrophic osteoarthropathy (HPOA) is
unclear. We presented a case of primary HPOA and performed a systematic review of …

Etoricoxib as a treatment of choice for patients with SLCO2A1 mutation exhibiting autosomal recessive primary hypertrophic osteoarthropathy: A case report

A Albawa'neh, MG Al Mansoori, S Diab… - Frontiers in …, 2022 - frontiersin.org
We reported a 22-year-old Emirati male with autosomal recessive primary hypertrophic
osteoarthropathy caused by a possibly pathogenic homozygous non-synonymous variant in …

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

Y Nakano, Y Ohata, M Fujiwara, T Kubota, Y Miyoshi… - Bone Reports, 2023 - Elsevier
Pachydermoperiostosis (PDP) is a rare hereditary disease characterized by digital clubbing,
pachydermia, and periostosis. We describe a Japanese male patient with PDP who was …

[HTML][HTML] Pachydermoperiostosis: a case report of initial improvement with etoricoxib

N Vaidya, N Acharya, S Katila, S Adhikari… - Annals of Medicine …, 2023 - journals.lww.com
Pachydermoperiostosis: a case report of initial improvement... : Annals of Medicine and
Surgery Pachydermoperiostosis: a case report of initial improvement with etoricoxib …

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

A Baniya, A Bhattarai, B Devkota, S Khatiwada… - Clinical Case …, 2023 - ncbi.nlm.nih.gov
Pachydermoperiostosis (PDP) is a rare genetic disorder with unclear etiopathogenesis. We
report a case of a 38‐year‐old male who presented with classic features of PDP. Our patient …

Pachydermoperiostosis Due to a Novel HPGD Splicing Site Mutation Masquerading as Acromegaly

M Almalki, B Alghamdi, A Benito, A Alfares… - JCEM Case …, 2024 - academic.oup.com
Abstract Hypertrophic osteoarthropathy (HOA: MIM 167100)) is classified into primary and
secondary types. Primary HOA, also known as pachydermoperiostosis (PDP), is a rare …

Coincidence of pachydermoperiostosis and synovitis, acne, pustulosis, hyperostosis, osteitis syndrome, a causal or casual association?

Y Feng, A Wang, X Dong, C Li, K Yuan… - International Journal …, 2022 - Wiley Online Library
Pachydermoperiostosis (PDP) is a rare disorder characterized by skin thickening,
acropachia, and periostosis. Synovitis, acne, pustulosis, hyperostosis, osteitis (SAPHO) …