Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review.

Children (Basel)

Pediatrics and Pediatric Emergency Department, University Hospital, A.O.U. "Policlinico-Vittorio Emanuele", 95100 Catania, Italy.

Published: August 2023

AI Article Synopsis

  • Klippel-Trenaunay syndrome is a rare congenital disorder defined by three main features: capillary malformations, varicosities, and tissue/bone hypertrophy, with diagnosis possible if at least two are present.
  • Capillary malformations are typically seen at birth, while varicosities and limb hypertrophy usually develop later, and while the syndrome is often benign, it can lead to serious complications in various organs.
  • Recent advancements categorize this syndrome under PIK3CA-related overgrowth spectrum disorders, with new insights into its genetic causes, clinical symptoms, potential complications, and management strategies for affected individuals.

Article Abstract

Klippel-Trenaunay syndrome is an uncommon, infrequent, congenital disorder characterized by a triad of capillary malformation, varicosities, and tissue and bone hypertrophy. The presence of two of these three signs is enough to obtain the diagnosis. Capillary malformations are usually present at birth, whereas venous varicosities and limb hypertrophy become more evident later. The syndrome has usually a benign course, but serious complications involving various organs, such as gastrointestinal and genitourinary organs, as well as the central nervous system, may be observed. Recently, Klippel-Trenaunay syndrome has been included in the group of PIK3CA-related overgrowth spectrum (PROS) disorders. In terms of this disorder, new results in etiopathogenesis and in modalities of treatment have been advanced. We report here a review of the recent genetic findings, the main clinical characteristics and related severe complications, differential diagnoses with a similar disorder, and the management of patients with this complex and uncommon syndrome.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453504PMC
http://dx.doi.org/10.3390/children10081421DOI Listing

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