Abstract
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 a differential diagnosis. In this article, we report a 17-year-old boy who presented with 2-year history of acral enlargement and facial appearance changes associated with joint pain and excessive sweating. He had been investigated extensively for acromegaly, and the final diagnosis was pachydermoperiostosis.
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CITATION STYLE
Abdullah, N. R. A., Jason, W. L. C., & Nasruddin, A. B. (2017). Pachydermoperiostosis: a rare mimicker of acromegaly. Endocrinology, Diabetes & Metabolism Case Reports, 2017. https://doi.org/10.1530/edm-17-0029
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