Pachydermoperiostosis
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| Pachydermoperiostosis Classification and external resources | |
| ICD-10 | L62.0, M89.4 |
|---|---|
| ICD-9 | 731.2, 757.39 |
Pachydermoperiostosis (PDP) is a rare disorder characterized by clubbing of the fingers, thickening of the skin of the face (pachyderma) and excessive sweating (hyperhidrosis). It was first described in 1868. However it wasn't until 1935, when Touraine-Solente-Golé recognised it as a syndrome.
In fact, there are 3 forms: 1. a complete form (pachydermia and periostosis), 2. an incomplete form (without pachydermia), and 3. a forme fruste (pachydermia with minimal-to-absent skeletal changes).
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Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
