Pachydermoperiostosis with Chronic Diarrhoea: A Case Report

Authors

  • Muhammad Shaista Ali Khan Assistant Professor (Medicine), Sheikh Hasina National Institute of Burn and Plastic Surgery, Dhaka, Bangladesh
  • Md Nahiduzzamane Shazzad Medical Officer, Department of Rheumatology, Bangabandhu Sheikh Mujib Medical University, Dhaka (BSMMU), Dhaka, Bangladesh
  • Shamim Ahmed Associate Professor, Department of Rheumatology, BSMMU, Dhaka, Bangladesh
  • Syed Atiqul Haq Professor, Department of Rheumatology, BSMMU, Dhaka, Bangladesh

DOI:

https://doi.org/10.3329/bmj.v50i3.62936

Keywords:

Pachydermoperiostosis, chronic diarrhea, Crohn’s disease

Abstract

Pachydermoperiostosis (PDP) is a rare autosomal disorder characterized by periostosis, clubbing, thickening of the skin (pachyderma) of the face and scalp, seborrhea and hyperhydrosis. It is the primary form of hypertrophic osteoarthropathy (HOA), the other name of which is Touraine- Solente-Golé syndrome. PDP has various organ involvements and there are some rare associations of PDP with other disorders. Here we describe a 16-year-old boy who presented with skin and skeletal manifestations typical of PDP who also had chronic diarrhea, abdominal pain and weight loss. After giving treatment with risedronate sodium and mesalazine he got significant improvement in his skeletal and abdominal complaints.

Bangladesh Med J. 2021 Sept; 50(3): 52-55

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Published

2022-11-23

How to Cite

Khan, M. S. A. ., Shazzad, M. N. ., Ahmed, S. ., & Haq, S. A. . (2022). Pachydermoperiostosis with Chronic Diarrhoea: A Case Report. Bangladesh Medical Journal, 50(3), 52–55. https://doi.org/10.3329/bmj.v50i3.62936

Issue

Vol. 50 No. 3 (2021)

Section

Case Reports