Sindrome de touraine-solente-goule. (paquidermoperiostosis primaria). reporte de un caso [PDF]
Medimay, 2008 Se presenta un caso de 37 años de edad con diagnóstico de Paquidermoperiostosis primaria o Síndrome de Touraine-Solente-Goulé, afección infrecuente, caracterizada por Paquidermia, Periostosis y Paquidactilia, que puede ser idiopática, con inicio en la ...
Eduardo Rivero Reyes
doaj +6 more sources
Primary hypertrophic osteoarthropathy – a rare cause of pain and arthritis in children. Description of 5 cases [PDF]
Central European Journal of Immunology, 2022 Primary hypertrophic osteoarthropathy (PHOA) is a very rare disease. The typical triad of symptoms, i.e. digital clubbing, periosteal bone formation with bone and joint deformities and skin hypertrophy, may be accompanied by other specific conditions. In
Joanna Wójtowicz +3 more
doaj +2 more sources
Pachydermo-periostosis (Idiopathic Osteoarthropathy) [PDF]
BMJ: British Medical Journal, 1957 exaly +3 more sources
A case report of an extremely rare association of ankylosing spondylitis with pachydermoperiostosis. [PDF]
Clin Case Rep, 2023 Key Clinical Message We describe a case of a young man with features of pachydermoperiostosis and spondyloarthropathy. By describing this rarity, we aim to help build a database for future studies and construct a management plan that rheumatologists and clinicians can use.
Gorial FI, Awadh NI, Hamzah MA.
europepmc +2 more sources
Familial complete pachydermoperiostosis presenting with vertebral hypertrophy and myelopathy [PDF]
JBMR PlusYuri A Zarate, Hartmut H Malluche
exaly +2 more sources
Hypertrophic Osteopathy Associated with Lung Adenocarcinoma in a Cat: An Overview
Acta Veterinaria, 2023 Hypertrophic osteopathy (HO) is a pathological condition characterized by progressive, bilateral and symmetrical periosteal bone hyperostosis. Hypertrophic osteopathy is considered a secondary disease that occurs as a consequence of many chronic ...
Janevski Aleksandar +5 more
doaj +1 more source
Pachydermoperiostosis combined with pyloric gland adenoma with foveolar-type adenoma. [PDF]
United European Gastroenterol JUnited European Gastroenterology Journal, Volume 12, Issue 1, Page 152-154, February 2024.
Long B, Jiang C, Zheng Q, Wan P.
europepmc +2 more sources
Bilateral Ptosis Due to a Rare Cause-Pachydermoperiostosis [PDF]
Journal of Clinical and Diagnostic Research, 2013 Pachydermoperiostosis is a rare hereditary disorder that is characterised by pachydermia (thickening of the facial skin and/ or scalp), and periostosis (swelling of the periarticular tissue and a subperiosteal new bone formation).
Mahesh M, K V K S N Murthy
doaj +1 more source
Complete form of pachydermoperiostosis, [PDF]
Anais 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 +1 more source
Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report
Clinical Case Reports, Volume 11, Issue 6, June 2023., 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
Abinash Baniya +6 more
wiley +1 more source