A Complete Form of Pachydermoperiostosis Accompanied by a Pituitary Microadenoma

Yan Jing Chen, Li Li Department of Dermatology and Venereology, West China Hospital, Sichuan University, Chengdu, Sichuan, People's Republic of ChinaCorrespondence: Li Li, Department of dermatology and venereology, West China Hospital, Sichuan University, Guoxue Alley No. 37, Wuhou District, Ch...

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Hoofdauteurs: Chen YJ (Auteur), Li L (Auteur)
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Gepubliceerd in: Dove Medical Press, 2023-01-01T00:00:00Z.
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100 1 0 |a Chen YJ  |e author 
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245 0 0 |a A Complete Form of Pachydermoperiostosis Accompanied by a Pituitary Microadenoma 
260 |b Dove Medical Press,   |c 2023-01-01T00:00:00Z. 
500 |a 1178-7015 
520 |a Yan Jing Chen, Li Li Department of Dermatology and Venereology, West China Hospital, Sichuan University, Chengdu, Sichuan, People's Republic of ChinaCorrespondence: Li Li, Department of dermatology and venereology, West China Hospital, Sichuan University, Guoxue Alley No. 37, Wuhou District, Chengdu, Sichuan, 610041, People's Republic of China, Tel +86 18980601692, Email lilihx_scu@scu.edu.cnAbstract: Pachydermoperiostosis is a rare genetic disease that is associated with HPGD (15-hydroxyprostaglandin dehydrogenase) and SLCO2A1 (solute carrier organic anion transporter family member 2A1) gene mutations. It is characterized by three major phenotypes, namely, pachydermia, periostosis, and digital clubbing. Clinically, misdiagnoses such as acromegaly and thyroid acropachy are commonly confused with pachydermoperiostosis. Integral medical history, physical examination, endocrinological tests, and multiple disciplinary cooperation are extremely significant in the accurate diagnosis of pachydermoperiostosis. The co-existence of pachydermoperiostosis and pituitary adenoma is rarely recorded and discussed. In this case, we present a young male patient with a complete form of pachydermoperiostosis and a nonfunctional pituitary microadenoma, which has rarely been reported.Keywords: pachydermoperiostosis, pituitary microadenoma, acromegaly, thyroid acropachy 
546 |a EN 
690 |a pachydermoperiostosis 
690 |a pituitary microadenoma 
690 |a acromegaly 
690 |a thyroid acropachy 
690 |a Dermatology 
690 |a RL1-803 
655 7 |a article  |2 local 
786 0 |n Clinical, Cosmetic and Investigational Dermatology, Vol Volume 16, Pp 47-52 (2023) 
787 0 |n https://www.dovepress.com/a-complete-form-of-pachydermoperiostosis-accompanied-by-a-pituitary-mi-peer-reviewed-fulltext-article-CCID 
787 0 |n https://doaj.org/toc/1178-7015 
856 4 1 |u https://doaj.org/article/b0f5bf0d048e4611b8716a2ee3e20683  |z Connect to this object online.