Results 11 to 20 of about 2,068 (238)

Complete form of pachydermoperiostosis, [PDF]

open access: goldAnais Brasileiros de Dermatologia, 2020
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
Mônica Larissa Padilha Honório   +2 more
doaj   +6 more sources

Familial complete pachydermoperiostosis presenting with vertebral hypertrophy and myelopathy. [PDF]

open access: goldJBMR Plus
Pachydermoperiostosis (PDP) is a rare, male-predominant (9:1) primary hypertrophic osteoarthropathy of the skin and bone, commonly called the acromegaly mimic.
Honaker E   +8 more
europepmc   +3 more sources

Pachydermoperiostosis: Three Case Reports [PDF]

open access: goldJournal 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
doaj   +4 more sources

Pachydermoperiostosis with bilateral ptosis and its associated systemic comorbidities: a rare case report. [PDF]

open access: yesPan Afr Med J, 2023
Pachydermoperiostosis is a rare genetic disease known as primary or idiopathic hypertrophic osteoarthropathy (HOA)/Touraine-Solente-Gole syndrome. It is an autosomal dominant or recessive disorder comprising digital clubbing, periostosis, hyperhidrosis ...
Hlaing SS   +8 more
europepmc   +2 more sources

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

open access: yesAnn Med Surg (Lond), 2023
Introduction and importance: Pachydermoperiostosis (PDP) is a syndrome characterised by the triad of pachydermia, digital clubbing and periostosis of long bones and its scarce incidence and similarity in clinical features with acromegaly makes the ...
Vaidya N   +4 more
europepmc   +2 more sources

Pachydermoperiostosis and Work Restrictions: A Case Report. [PDF]

open access: yesCureus, 2023
Pachydermoperiostosis (PDP) is a rare disease that mimics the clinical and radiographical manifestations of acromegaly. Therefore, it should be considered as one of the differential diagnoses in the evaluation of acromegalic patients.
Chinichian M   +3 more
europepmc   +2 more sources

Pachydermoperiostosis Presenting With End-Stage Kidney Disease. [PDF]

open access: yesCureus
Pachydermoperiostosis, also known as Touraine-Solente-Golé syndrome, is an uncommon hereditary condition. This condition includes skin thickening (pachydermia), abnormalities of the bones (periostosis), and digital clubbing (acropachy). We present a case
Ghai HK, Suresh S, Elumalai RP.
europepmc   +2 more sources

Complete pachydermoperiostosis with diffuse keratoderma mimicking thyroid Acropachy: A case report and review of literature

open access: yesIbom Medical Journal, 2023
Pachydermoperiostosis (PDP) is a rare genodermatosis with prominent cutaneous, soft tissue and skeletal manifestations. It can mimic secondary causes of hypertrophic osteoarthropathy such as thyroid acropachy.
Ajani AA   +5 more
doaj   +2 more sources

Pachydermoperiostosis Due to a Novel HPGD Splicing Site Mutation Masquerading as Acromegaly. [PDF]

open access: yesJCEM Case Rep
Hypertrophic osteoarthropathy (HOA: MIM 167100)) is classified into primary and secondary types. Primary HOA, also known as pachydermoperiostosis (PDP), is a rare genetic condition with distinct clinical features including digital clubbing, skin ...
Almalki M   +4 more
europepmc   +2 more sources

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