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Multimodality imaging approach in a patient with Klippel-Trenaunay syndrome. | LitMetric

AI Article Synopsis

  • Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder characterized by asymmetric limb overgrowth, skin capillary malformations, and varicose veins, primarily in the lower limbs.
  • A case study of a 27-year-old man illustrates typical symptoms of KTS, including enlarged varicosities, significant asymmetry in limb size, and distinct skin markings.
  • Diagnostic imaging techniques such as Doppler ultrasound, CT angiograms, and MRI are essential for diagnosing KTS and distinguishing it from other similar conditions.

Article Abstract

Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder presenting with asymmetric limb hypertrophy, cutaneous capillary malformations and lower extremity varicosities. We discuss a 27-year-old man born with varicosities on both lower extremities, which progressively enlarged. Physical examination showed a grossly enlarged right hand. There were multiple compressible varicosities, diffuse port-wine stains on the right leg and limb-length discrepancy on the left leg. CT angiogram and Doppler ultrasound revealed several venous varicosities. Ectatic veins in the right leg converge into the lateral marginal vein of Servelle, an embryonic vein, typically seen in KTS patients. KTS is diagnosed clinically and imaging plays a role in differentiating this from other disease entities that present similarly. Doppler ultrasound is the initial imaging of choice to characterise varicosities and to identify thrombosis and reflux. Plain radiographs confirm limb hypertrophy. MRI and CT angiograms are useful to evaluate vascular anomalies and its accompanying soft tissue changes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706670PMC
http://dx.doi.org/10.1136/bcr-2018-228257DOI Listing

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