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
Daniel José Dias Cunha +4 more
doaj +3 more sources
Pachydermodactyly: An Underdiagnosed Condition in Adolescence—A Case Report and Literature Review [PDF]
Pachydermodactyly (PDD) is a rare, underdiagnosed benign condition characterized by asymmetrical, bilateral fusiform swellings of the hands’ proximal interphalangeal (PIP) joints.
Mishari T. Alrubaiaan +2 more
doaj +3 more sources
Pachydermoperiostosis combined with pyloric gland adenoma with foveolar-type adenoma. [PDF]
United European Gastroenterology Journal, Volume 12, Issue 1, Page 152-154, February 2024.
Long B, Jiang C, Zheng Q, Wan P.
europepmc +3 more sources
JEADV Clinical Practice, Volume 4, Issue 1, Page 277-280, March 2025.
Tomoya Takegami +13 more
doaj +3 more sources
Pachydermoperiostosis Associated With a Rare SLCO2A1 Mutation: A Case Report and Literature Review. [PDF]
Pachydermoperiostosis (PDP), also known as primary hypertrophic osteoarthropathy, is a rare genetic disorder characterized by digital clubbing, periostosis, and pachydermia.
Mohammad M +6 more
europepmc +2 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 +2 more sources
Pachydermoperiostosis: a rare mimicker of acromegaly [PDF]
Pachydermoperiostosis is a very rare osteoarthrodermopathic disorder whose clinical and radiographic presentations may mimic those of acromegaly. In the evaluation of patients with acromegaloid appearances, pachydermoperiostosis should be considered as
Noor Rafhati Adyani Abdullah +2 more
doaj +3 more sources
Endocrine Alterations in Patients With Pachydermoperiostosis.
Context Pachydermoperiostosis (primary hypertrophic osteoarthropathy, PHO), usually due to biallelic loss of function variants in HPGD and SLCO2A1, has some features overlapping with acromegaly and is often referred to endocrinologists.
Stelmachowska-Banaś M +21 more
europepmc +2 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 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

