The primary hypertrophic osteoarthropathy (PHOA) (pachydermoperiostosis) is a rare genetic/hereditary disease characterized by skin changes (pachydermia), clubbing of fingers and periosteal thickening (periostitis) with sub-periosteal new bone formation.
Sivathapandi T +3 more
europepmc +5 more sources
Touraine Solente Gole Syndrome (Pachydermoperiostosis): Case Report and Brief Review
Observation: Hypertrophic osteoarthropathy (HOA) is systemic disease characterized by periostosis, digital clubbing and arthritis. Touraine Solente Gole syndrome (TSGS), or pachydermoperiostosis clinical variant of primary HOA, involving skeleton, soft ...
Zulfuqar Hasan Farajev +5 more
semanticscholar +3 more sources
Touraine-Solente-Gole Syndrome. (Primary paquidermoperiostosis). Two case report
Two cases occur in the same family (siblings) of 30 and 16 years of age with a diagnosis of primary pachydermoperiostosis or Touraine-Solente-Goulé Syndrome (TSG), an uncommon condition, characterized by pachydermia, periostosis and pachydactyly, which ...
Martha Mengana Medina +3 more
semanticscholar +5 more sources
Touraine-Solente-Gole Syndrome- A Rare Cause of Familial Periostosis [PDF]
Ajay Sharawat +3 more
semanticscholar +4 more sources
Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report. [PDF]
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
europepmc +2 more sources
Frontal lifting using a tissue expander in pachydermoperiostosis: A case report. [PDF]
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
europepmc +2 more sources
Pachydermoperiostosis (Touraine–Solente–Gole syndrome) imitating Acromegaly
Pachydermoperiostosis (PDP), also known as Touraine-Solente-Golé syndrome/Rosenfeld-Kloepfer syndrome/primary or idiopathic Hypertrophic osteoarthropathy, is an autosomal-dominant/autosomal recessive inherited disorder with variable expression.
R. Gomes
semanticscholar +2 more sources
Touraine Solente Gole Syndrome – The disease and associated Tongue fissuring
G. Athappan +5 more
semanticscholar +3 more sources
Touraine-Solente-Gole syndrome with acne vulgaris successfully treated with isotretinoin [PDF]
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 ...
A. C. Souza +6 more
semanticscholar +2 more sources
Primary Idiopathic Osteoarthropathy: Could It Be Related to Alcoholism? [PDF]
Background. Hypertrophic osteoarthropathy (HOA) is a syndrome characterized by abnormal proliferation of the skin and bony structures at the distal extremities resulting in digital clubbing, periosteal bony reaction, and joint effusion. It can be primary (idiopathic) without any clear identifiable etiology as well as secondary to variety of systemic ...
Alnimer Y +3 more
europepmc +2 more sources

