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Klippel-Trenaunay Syndrome - DOAJ

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Last Updated: 01 May 2022

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Chronic lower extremity wounds in a patient with Klippel Trenaunay syndrome

Klippel-Trenaunay syndrome, a rare disorder characterized by the triad of vascular and/or lymphatic malformations, capillary malformations, and soft tissue or bony hypertrophy. We present the case of a 46-year-old man with persistent lower extremity ulcers that are unresponsive to wound care therapy in this case report.

Source link: https://doi.org/10.1016/j.jvscit.2018.11.003


Clinical Experience of the Klippel-Trenaunay Syndrome

Three cellular triady malformations, venous malformations, and soft tissue and/or bony hypertrophy of the extremities are all typical of Klippel-Trenaunay syndrome. paraphrasedoutput:MethodsWe investigated a retrospective review of 19 patients with KTS and treated in our vascular anomalies clinic between 2003 and 2014, examining their demographics, their clinical characteristics, and the medications administered. ResultsUnderstanded The sex distribution was uneven, with 9 males and ten females. Plastic surgeons who are not careful tend to attach a one-sided importance to common conditions such as leg hypertrophy or capillary malformation, but skip other signs and medical characteristics. In all infants with capillary malformations or leg hypertrophy that require a multi-disciplinary approach for comprehensive management, KTS can be suspected.

Source link: https://doi.org/10.5999/aps.2015.42.5.552


A Case of Femoral Fracture in Klippel Trenaunay Syndrome

We discuss Klippel Trenaunay syndrome, a condition that has caused severe bilateral knee osteoarthritis in patients. paraphysis fracture while on the waiting list, the patient suffered a fall and sustained complete femoral diaphysis fracture. In KTS, there are only two recent reports of femoral fractures. This is the first report of a patient with this rare condition being treated with this therapy. In this large group of patients, we address fracture prevention.

Source link: https://doi.org/10.1155/2014/548161


Successful Management of Pregnancy Complicated by Klippel-Trenaunay Syndrome Using MR Angiography-Based Evaluation

With a normal coagulation profile, hypertrophy and multiple venous varicosities of her leg, as well as massive vulvovaginal varicosities, became prominent with a 35-week age. Hemangiomas and varicosities were found in the right leg, the lower abdomen, and the pubic area, according to Systematic MRAs, although no apparent AVM was found around the bronchial tube and spine. A healthy baby was born after we decided to have her baby by cesarean section at 37 weeks under general anesthesia.

Source link: https://doi.org/10.1155/2011/723467


Klippel Trenaunay Syndrome: A Brief Overview

B S T R A T C Klippel-Trenaunay syndrome is a rare congenital vascular disease. Although the number of cases is small, a doctor must be able to distinguish Klippel-Trenaunay Syndrome from other rare vascular disorders. Parkes Weber syndrome is usually similar to Klippel-Trenaunay syndrome, except in the arterial malformations related to capillary malformations and soft tissue to skeletal or bone hypertrophy. There are several options in relation to the treatment of Klippel-Trenaunay Syndrome (Trenay Syndrome), and non-invasive surgery is considered to be the most common of therapy options.

Source link: https://doi.org/10.32539/bsm.v5i2.231

* Please keep in mind that all text is summarized by machine, we do not bear any responsibility, and you should always check original source before taking any actions

* Please keep in mind that all text is summarized by machine, we do not bear any responsibility, and you should always check original source before taking any actions