Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report

被引：3

作者：

Baniya, Abinash ^{[1
,2
]}

Bhattarai, Ayam ^{[1
]}

Devkota, Bibek ^{[1
]}

Khatiwada, Saurav ^{[1
]}

Kafle, Pramod Kumar ^{[1
]}

Phuyal, Achyut Krishna ^{[1
]}

Shahi, Manoj ^{[1
]}

机构：

[1] Chitwan Med Coll, Bharatpur, Nepal

[2] Chitwan Med Coll, Bharatpur, Chitwan, Nepal

来源：

CLINICAL CASE REPORTS | 2023年 / 11卷 / 06期

关键词：

clubbing; etoricoxib; osteoarthropathy; pachydermoperiostosis; PRIMARY HYPERTROPHIC OSTEOARTHROPATHY; MUTATION; BONE; PROSTAGLANDINS; RECEPTOR; DISEASE;

D O I：

10.1002/ccr3.7526

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Key Clinical MessagePachydermoperiostosis 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. Pachydermoperiostosis (PDP) is a rare genetic disorder with unclear etiopathogenesis. We report a case of a 38-year-old male who presented with classic features of PDP. Our patient showed a good initial response to etoricoxib therapy but the safety and efficacy over long-term use are yet to be determined in further studies.

引用

页数：7

共 41 条

[1] Touraine Solente Gole syndrome: the disease and associated tongue fissuring [J].

Athappan, Ganesh ;

Unnikrishnan, Athira ;

Chengat, Vipindas ;

Chandraprakasam, Satish ;

Arthanareeswaran, Vinodhkumaradithya ;

Muthukrishnan, Srinivasan ;

Ponniyah, Thirumalaikolundusubramanian .

RHEUMATOLOGY INTERNATIONAL, 2009, 29 (09) :1091-1093

[2]

Auger DM., PACHYDERMOPERIOSTOSI

[3]

Bhansali A, 2006, J Assoc Physicians India, V54, P340

[4]

Borochowitz Z., 1990, BIRTH DEFECTS ENCY, P1349

[5] HYPERTROPHIC OSTEOARTHROPATHY IN PORTAL CIRRHOSIS [J].

BUCHAN, DJ ;

MITCHELL, DM .

ANNALS OF INTERNAL MEDICINE, 1967, 66 (01) :130-+

[6] Pachydermoperiostosis: an update [J].

Castori, M ;

Sinibaldi, L ;

Mingarelli, R ;

Lachman, RS ;

Rimoin, DL ;

Dallapiccola, B .

CLINICAL GENETICS, 2005, 68 (06) :477-486

[7] The hippocratic finger points the blame at PGE2 [J].

Coggins, Kenneth G. ;

Coffman, Thomas M. ;

Koller, Beverly H. .

NATURE GENETICS, 2008, 40 (06) :691-692

[8] A novel recessive 15-hydroxyprostaglandin dehydrogenase mutation in a family with primary hypertrophic osteoarthropathy [J].

Erken, Eren ;

Koroglu, Cigdem ;

Yildiz, Fatih ;

Ozer, Huseyin T. E. ;

Gulek, Bozkurt ;

Tolun, Aslihan .

MODERN RHEUMATOLOGY, 2015, 25 (02) :315-321

[9] Treatment of pachydermoperiostosis pachydermia with botulinum toxin type A [J].

Ghosn, Samer ;

Uthman, Imad ;

Dahdah, Maurice ;

Kibbi, Abdul Ghani ;

Rubeiz, Nelly .

JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2010, 63 (06) :1036-1041

[10] HYPERTROPHIC OSTEOARTHROPATHY SECONDARY TO UPPER-GASTROINTESTINAL-TRACT NEOPLASM - CASE REPORT AND REVIEW [J].

HOLLIS, WC .

ANNALS OF INTERNAL MEDICINE, 1967, 66 (01) :125-+

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