2023
DOI: 10.7759/cureus.36675
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Pachydermoperiostosis and Work Restrictions: A Case Report

Abstract: 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. In this study, we discussed a case of PDP in a 24-year-old simple worker working in a food industry factory and reviewed the work restrictions caused by the complications of the disease.

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“…The widening of the transverse diameter of the bone results from increased osteogenesis, and histology has simultaneously demonstrated elevated collagen formation and elevated urinary excretion of hydroxyproline in pachydermoperiostosis ( 39 ). The responsible genes, hydroxyprostaglandin dehydrogenase (HPGD) and solute carrier organic anion transporter family member 2A1 (SLCO2A1), have been identified, leading to an understanding of the etiology and the development of treatment for skin and bone hypertrophy ( 37 , 38 ). Genetics have been found to link the increase/decrease in skin collagen with the increase/decrease in bone formation.…”
Section: Similarities Between Skin and Bonementioning
confidence: 99%
“…The widening of the transverse diameter of the bone results from increased osteogenesis, and histology has simultaneously demonstrated elevated collagen formation and elevated urinary excretion of hydroxyproline in pachydermoperiostosis ( 39 ). The responsible genes, hydroxyprostaglandin dehydrogenase (HPGD) and solute carrier organic anion transporter family member 2A1 (SLCO2A1), have been identified, leading to an understanding of the etiology and the development of treatment for skin and bone hypertrophy ( 37 , 38 ). Genetics have been found to link the increase/decrease in skin collagen with the increase/decrease in bone formation.…”
Section: Similarities Between Skin and Bonementioning
confidence: 99%