Clinical Case Reports (Jun 2023)

Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report

  • Abinash Baniya,
  • Ayam Bhattarai,
  • Bibek Devkota,
  • Saurav Khatiwada,
  • Pramod Kumar Kafle,
  • Achyut Krishna Phuyal,
  • Manoj Shahi

DOI
https://doi.org/10.1002/ccr3.7526
Journal volume & issue
Vol. 11, no. 6
pp. n/a – n/a

Abstract

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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 showed a good initial response in our patient. Abstract Pachydermoperiostosis (PDP) is a rare genetic disorder with unclear etiopathogenesis. We report a case of a 38‐year‐old male who presented with classic features of PDP. Our patient showed a good initial response to etoricoxib therapy but the safety and efficacy over long‐term use are yet to be determined in further studies.

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