Results 11 to 20 of about 2,068 (238)
Complete form of pachydermoperiostosis, [PDF]
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]
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]
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 complicated with psoriatic arthritis successfully treated with an anti-interleukin 17A antibody [PDF]
Kyoko Sugioka, MD+2 more
doaj +3 more sources
Pachydermoperiostosis with bilateral ptosis and its associated systemic comorbidities: a rare case report. [PDF]
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]
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]
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]
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
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]
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