Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/32450
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dc.contributor.authorRozeta SOKOLOVAen_US
dc.contributor.authorNjomza LUMANI-BAKIJIen_US
dc.contributor.authorLazo JOVCHESKIen_US
dc.contributor.authorAleksandar STEPANOVSKIen_US
dc.date.accessioned2025-02-11T11:33:32Z-
dc.date.available2025-02-11T11:33:32Z-
dc.date.issued2023-05-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/32450-
dc.description17 – 19 May, 2023 Tetovo, Republic of North Macedoniaen_US
dc.description.abstractIntroduction: Lymphatic malformations (LM) are congenital benign malformations from the group of slow-flow vascular anomalies consisting of pathological cystic dilatation of the lymphatic vessels. The incidence of LM ranges from 1.5 to 2.8% in 2000 to 4000 newborn children, and are relatively rare congenital vascular anomalies. They are characterized with equal representation between the genders. From the structural aspect, LM are divided into macrocystic, microcystic and mixed type, with its own therapeutic and prognostic implications. A small percentage of LM are combined with additional anomalies and are part of syndromes such as CLOVES, Klippel-Trenaunay, Proteus and others. In recent years, the method of choice in the treatments is sclerosing as a non-invasive method achieving almost excellent results.en_US
dc.language.isoenen_US
dc.publisherUniversity of Tetovoen_US
dc.subjectlymphatic malformationsen_US
dc.subjectminimally invasive methoden_US
dc.subjectsclerotherapyen_US
dc.subjectsclerosing agenten_US
dc.subjectpediatric populationen_US
dc.titleTREATMENT OF LYMPHATIC MALFORMATIONS IN CHILDREN: 3 YEARS EXPERIENCEen_US
dc.typeProceeding articleen_US
dc.relation.conferenceInternational Congress on Natural, Health Sciences and Technologyen_US
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Appears in Collections:Faculty of Medicine: Conference papers
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