ArticleCureus2022
A Rare Case of Klippel-Trénaunay Syndrome.
Article in Cureus, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 5 citations in OpenAlex.
- Extensive venolymphatic involvement in infantile Klippel-Trenaunay syndrome: A rare case from Ethiopia.Radiology case reports · 2025Article
- Klippel-Trenaunay syndrome in a child presented with bladder hemangioma: a rare manifestation of a rare syndrome.Annals of medicine and surgery (2012) · 2025Article
- Isolated Colorectal Involvement in Klippel-Trenaunay Syndrome: A Case of Extensive Vascular Malformation.International medical case reports journal · 2025Article
- Large birth mark and unilateral swelling of the lower extremity in a young teenager.BMJ case reports · 2024Article
- A Multiple Synergic Treatment for Non-Healing Ulcer Management in a Patient withReports (MDPI) · 2023Article
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Authors and funding
6 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The Klippel-Trénaunay syndrome (KTS) is a rare form of a birth disorder that includes capillary malformation, hypertrophy of bones and soft tissues, and tortuous varicosities, as well as hypertrophy of the capillaries resulting in hemangiomas and port wine discoloration. KTS is also known as angio-osteohypertrophy syndrome and dysplastic angiopathy. In this case report, we describe the case of a 13-year-old female with multiple superficial varicosities on the medial aspect of her left leg since birth. Computed tomography angiogram assessed and identified abnormal venous drainage in the lower limb. Klippel-Trénaunay-Weber syndrome (KTWS) differs from KTS in that KTWS involves arteriovenous malformations.
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Registered trials
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