Zobrazeno 1 - 10
of 477
pro vyhledávání: '"pachydermoperiostosis"'
Publikováno v:
Case Reports in Dermatology, Vol 16, Iss 1, Pp 63-69 (2024)
Introduction: Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy, is a rare autosomal dominant disease with primary clinical features of pachydermia (thickening of skin) and periostosis (new bone formation). Keloid scar formation i
Externí odkaz:
https://doaj.org/article/35f6acdb27e64c07972f4b6fafe84ee3
Publikováno v:
罕见病研究, Vol 2, Iss 4, Pp 523-528 (2023)
Objective To analyze the clinical characteristics, treatments and prognosis of pachydermoperiostosis (PDP) with synovitis, and to improve clinicians′ understanding of PDP. Methods The clinical data of 5 patients diagnosed with PDP in Peking Union M
Externí odkaz:
https://doaj.org/article/0afef7f278014d1f9b66d820229c0707
Akademický článek
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Autor:
AKM Kamruzzaman, Maisha Farzana, Md Mainuddin Sohel, Emrul Kaiser, Nobendu Chowdhury, Md Hafizur Rahman, Syed Atiqul Haq, Johannes J. Rasker
Publikováno v:
Rheumato, Vol 3, Iss 1, Pp 98-105 (2023)
Pachydermoperiostosis (PDP), also called primary hypertrophic osteoarthropathy (HOA), is a rare genetic disease with typical thickening of the skin (pachydermia) and rheumatic manifestations, with clubbing of the fingers and toes and periostosis of t
Externí odkaz:
https://doaj.org/article/cd8cb06e25364ac28d8424204b557aaa
Publikováno v:
Clinical, Cosmetic and Investigational Dermatology, Vol Volume 16, Pp 47-52 (2023)
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 Univ
Externí odkaz:
https://doaj.org/article/b0f5bf0d048e4611b8716a2ee3e20683
Publikováno v:
JAAD Case Reports, Vol 35, Iss , Pp 43-45 (2023)
Externí odkaz:
https://doaj.org/article/6ba50e73fde44ef59e494717a14135d0
Autor:
Emine Kartal Baykan, Ayberk Türkyılmaz
Publikováno v:
JCRPE, Vol 14, Iss 3, Pp 350-355 (2022)
Pachydermoperiostosis (PDP), also known as primary hypertrophic osteoarthropathy, is a rare genetic disorder characterized by pachyderma and periostosis. Acromegaly is a condition caused by excessive secretion of growth hormone (GH) leading to elevat
Externí odkaz:
https://doaj.org/article/be411da88b0248169bab283b5a471214
Autor:
Abinash Baniya, Ayam Bhattarai, Bibek Devkota, Saurav Khatiwada, Pramod Kumar Kafle, Achyut Krishna Phuyal, Manoj Shahi
Publikováno v:
Clinical Case Reports, Vol 11, Iss 6, Pp n/a-n/a (2023)
Key Clinical Message Pachydermoperiostosis is a rare genetic disorder that closely resembles acromegaly. Diagnosis is usually based on distinct clinical and radiological features. Oral etoricoxib therapy showed a good initial response in our patient.
Externí odkaz:
https://doaj.org/article/345585c3ceb8495bbf3340f4a987e725
Publikováno v:
Bone Reports, Vol 18, Iss , Pp 101673- (2023)
Pachydermoperiostosis (PDP) is a rare hereditary disease characterized by digital clubbing, pachydermia, and periostosis. We describe a Japanese male patient with PDP who was differentially diagnosed with acromegaly by identification of compound hete
Externí odkaz:
https://doaj.org/article/407b3d0dbaa64da39e9e5990edc8c84f
Publikováno v:
Clinical Case Reports, Vol 11, Iss 5, Pp n/a-n/a (2023)
Key Clinical Message We describe a case of a young man with features of pachydermoperiostosis and spondyloarthropathy. By describing this rarity, we aim to help build a database for future studies and construct a management plan that rheumatologists
Externí odkaz:
https://doaj.org/article/66da7e3cf2ea46a296dc3650f41b71b8