Klippel-trenaunay syndrome in a child with coexisting lymphangioma, vascular insufficiency, and multiple soft tissue swellings: a case report
In conclusion, KTS is a challenging disease due to its rarity, diagnostic complexity, and varied clinical manifestations. It can be presented with different manifestations and complications, hence makes it very difficult for clinicians to diagnose. For the growing awareness, new research can enhance the knowledge of the clinician about the disease and provide better care for the individuals afflicted by KTS.
Authors
- Inibehe Ime Okon (ORCID: https://orcid.org/0009-0003-8275-5713)
- Syed Ali Arsal (ORCID: https://orcid.org/0000-0002-8665-4288)
- Muhammad Aniq Amir
- Muhammad Amir (ORCID: https://orcid.org/0009-0000-6394-4509)
- Oluwatobiloba Israel Popoola
- Rameez Hussain
- Ahmed Ibrahim Siddiqui
- Saif Ullah Bin Bilal
Institutions
- Shenyang Medical College (CN)
- Karachi Medical and Dental College (PK)
- Jinnah Sindh Medical University (PK)
- Shaheed Mohtarma Benazir Bhutto Medical University (PK)
- Green Circle (CZ)
Publication Details
- Journal
- Oxford Medical Case Reports
- Published
- 2025-12-04
- DOI
- https://doi.org/10.1093/omcr/omaf286
- Primary Topic
- Vascular Malformations and Hemangiomas
- Type
- article
- Field-Weighted Citation Impact
- 0.00