Pachydermoperiostosis (Touraine-Solente–Gole Syndrome): A Case Report of Primary Hypertrophic Osteoarthropathy
Background: Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy (PHO), also known as the Touraine–Solente–Gole syndrome, is a genetic disorder that is uncommon and is identified by finger clubbing, skin thickening, and periosteal growth. Case Report: This case study details the cas...
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| Format: | Article |
| Language: | English |
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World Scientific Publishing
2024-01-01
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| Series: | Journal of Clinical Rheumatology and Immunology |
| Online Access: | https://www.worldscientific.com/doi/10.1142/S2661341724740791 |
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| author | Asif Islam Kinza Shahid Fatima Khurshid Memoona Khalood |
| author_facet | Asif Islam Kinza Shahid Fatima Khurshid Memoona Khalood |
| author_sort | Asif Islam |
| collection | DOAJ |
| description | Background: Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy (PHO), also known as the Touraine–Solente–Gole syndrome, is a genetic disorder that is uncommon and is identified by finger clubbing, skin thickening, and periosteal growth. Case Report: This case study details the case of a 21-year-old man with PDP to raise awareness, improve diagnosis, and enhance management strategies for the condition. The individual showed common signs like digital clubbing, pachydermia, and periostosis, as well as related symptoms like hyperhidrosis. Radiological imaging supported the diagnosis by revealing periosteal reactions and cortical thickening in multiple bones. Other conditions with comparable clinical characteristics were considered in the differential diagnosis, however, the diagnosis of PHO was confirmed by the specific radiological results and normal hormonal levels. The treatment primarily targets alleviating symptoms with drugs like NSAIDs and corticosteroids, along with newer options such as bisphosphonates. Conclusion: Timely detection and correct treatment are essential to enhance the well-being of people with PHO. This case study emphasizes the significance of tracking symptoms and offering thorough care to those with PDP/PHO. |
| format | Article |
| id | doaj-art-a895fde3ad4649ca87628dcbee278edc |
| institution | OA Journals |
| issn | 2661-3417 2661-3425 |
| language | English |
| publishDate | 2024-01-01 |
| publisher | World Scientific Publishing |
| record_format | Article |
| series | Journal of Clinical Rheumatology and Immunology |
| spelling | doaj-art-a895fde3ad4649ca87628dcbee278edc2025-08-20T02:14:14ZengWorld Scientific PublishingJournal of Clinical Rheumatology and Immunology2661-34172661-34252024-01-0124supp0112112110.1142/S2661341724740791Pachydermoperiostosis (Touraine-Solente–Gole Syndrome): A Case Report of Primary Hypertrophic OsteoarthropathyAsif Islam0Kinza Shahid1Fatima Khurshid2Memoona Khalood3Ali Fatima Hospital, Lahore, PakistanAli Fatima Hospital, Lahore, PakistanMirpur University of Science and Technology (MUST), PakistanAli Fatima Hospital, Lahore, PakistanBackground: Pachydermoperiostosis (PDP), or primary hypertrophic osteoarthropathy (PHO), also known as the Touraine–Solente–Gole syndrome, is a genetic disorder that is uncommon and is identified by finger clubbing, skin thickening, and periosteal growth. Case Report: This case study details the case of a 21-year-old man with PDP to raise awareness, improve diagnosis, and enhance management strategies for the condition. The individual showed common signs like digital clubbing, pachydermia, and periostosis, as well as related symptoms like hyperhidrosis. Radiological imaging supported the diagnosis by revealing periosteal reactions and cortical thickening in multiple bones. Other conditions with comparable clinical characteristics were considered in the differential diagnosis, however, the diagnosis of PHO was confirmed by the specific radiological results and normal hormonal levels. The treatment primarily targets alleviating symptoms with drugs like NSAIDs and corticosteroids, along with newer options such as bisphosphonates. Conclusion: Timely detection and correct treatment are essential to enhance the well-being of people with PHO. This case study emphasizes the significance of tracking symptoms and offering thorough care to those with PDP/PHO.https://www.worldscientific.com/doi/10.1142/S2661341724740791 |
| spellingShingle | Asif Islam Kinza Shahid Fatima Khurshid Memoona Khalood Pachydermoperiostosis (Touraine-Solente–Gole Syndrome): A Case Report of Primary Hypertrophic Osteoarthropathy Journal of Clinical Rheumatology and Immunology |
| title | Pachydermoperiostosis (Touraine-Solente–Gole Syndrome): A Case Report of Primary Hypertrophic Osteoarthropathy |
| title_full | Pachydermoperiostosis (Touraine-Solente–Gole Syndrome): A Case Report of Primary Hypertrophic Osteoarthropathy |
| title_fullStr | Pachydermoperiostosis (Touraine-Solente–Gole Syndrome): A Case Report of Primary Hypertrophic Osteoarthropathy |
| title_full_unstemmed | Pachydermoperiostosis (Touraine-Solente–Gole Syndrome): A Case Report of Primary Hypertrophic Osteoarthropathy |
| title_short | Pachydermoperiostosis (Touraine-Solente–Gole Syndrome): A Case Report of Primary Hypertrophic Osteoarthropathy |
| title_sort | pachydermoperiostosis touraine solente gole syndrome a case report of primary hypertrophic osteoarthropathy |
| url | https://www.worldscientific.com/doi/10.1142/S2661341724740791 |
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