Nosological Consideration of Arterial Aneurysms Associated with Klippel–Trenaunay Syndrome
Author:
Affiliation:
1. Department of Vascular Surgery, Daiyukai Daiichi Hospital
2. Department of Plastic and Reconstructive Surgery, Yokohama City University Hospital
Publisher
The Editorial Committee of Annals of Vascular Diseases
Link
https://www.jstage.jst.go.jp/article/avd/13/4/13_ra.20-00089/_pdf
Reference28 articles.
1. 1) Mulliken JB, Burrows PE, Fishman SJ eds. Mulliken & Young’s Vascular Anomalies. Hemangiomas and Malformations. Oxford, Oxford University Press, 2013, 29.
2. 2) Klippel M, Trenaunay P. Du naevus variqueux osteohypértrophique. Arch Gen Med 1900; 185: 641-72.
3. 3) https://www.issva.org/UserFiles/file/ISSVA-Classification-2018.pdf
4. 4) Kurek KC, Luks VL, Ayturk UM, et al. Somatic mosaic activating mutations in PIK3CA cause GLOVES syndrome. Am J Hum Genet 2012; 90: 1108-15.
5. 5) Lee A, Driscoll D, Gloviczki P, et al. Evaluation and management of pain in patients with Klippel–Trenaunay syndrome: a review. Pediatrics 2005; 115: 744-9.
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1. Options in the treatment of superficial and deep venous disease in patients with Klippel-Trenaunay syndrome;Journal of Vascular Surgery: Venous and Lymphatic Disorders;2022-11
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