Complete pachydermoperiostosis: A case report
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Mohd Firdaus Abdul Mubing 1 , Razlina Abdul Rahman 1 2 * , Salziyan Badrin 1 2 , Hasni Ibrahim 3
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1 Department of Family Medicine, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, MALAYSIA2 Hospital Universiti Sains Malaysia, Jalan Raja Perempuan Zainab 2, Kubang Kerian, Kelantan, MALAYSIA3 Klinik Kesihatan Gunong, Bachok, Kelantan, MALAYSIA* Corresponding Author

Abstract

Pachydermoperiostosis (PDP), also known as Touraine-Solente-Gole syndrome or primary hypertrophic osteoarthropathy, is a very rare disease mainly characterized by pachyderma, finger clubbing, hyperhidrosis, and periostosis. We reported a case of a patient who suffered from gradual pain and enlargement of both hands and feet for 25 years despite receiving treatment from multiple clinics. He also experienced gradual abnormal changes in his face and scalp. Radiographic images of the lower limbs revealed the presence of subperiosteal bone growth and periosteal hypertrophy. The diagnosis of complete PDP was made late due to its rarity and the unfamiliarity of medical practitioners with the diagnosis. This case highlighted the need for medical practitioners to be aware of rare diseases so that patients may be diagnosed and treated earlier and thereby relieving their anxiety and improve their quality of life.

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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Article Type: Case Report

ELECTRON J GEN MED, Volume 21, Issue 1, February 2024, Article No: em554

https://doi.org/10.29333/ejgm/13900

Publication date: 01 Jan 2024

Online publication date: 15 Nov 2023

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Article Downloads: 951

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