2010
DOI: 10.1016/j.otohns.2010.02.025
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Lymphatic malformations: Current cellular and clinical investigations

Abstract: The etiology and pathogenesis of head and neck lymphatic malformations are poorly understood, but understanding is improving through ongoing investigation. Reduction of lymphatic malformation size is generally possible, but further work is necessary to optimize methods for measuring therapeutic outcomes in problematic areas.

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Cited by 101 publications
(79 citation statements)
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“…The main aim of lymphatic malformation treatment is to restore and preserve the function and aesthetic integrity [13]. Treatment of lymphatic malformations is difficult; Because they impregnate to the surrounding tissues, specially the microcystic type of tongue lymphatic malformations considered as a challenging one, it can range from surgical excision, sclerotherapy, cryotherapy, electrocautery, corticosteroid injection, and embolization [14,15].…”
Section: Discussionmentioning
confidence: 99%
“…The main aim of lymphatic malformation treatment is to restore and preserve the function and aesthetic integrity [13]. Treatment of lymphatic malformations is difficult; Because they impregnate to the surrounding tissues, specially the microcystic type of tongue lymphatic malformations considered as a challenging one, it can range from surgical excision, sclerotherapy, cryotherapy, electrocautery, corticosteroid injection, and embolization [14,15].…”
Section: Discussionmentioning
confidence: 99%
“…Jugular lymphatic obstruction sequence, abnormal embryonic sequestration of lymphatic tissue, or abnormal budding of the lymphatics results in cystic hygroma formation 6,8,9 . Vascular endothelial growth factor C (VEGF -C) is postulated to play role in lymphatic malformations 10 . About 78% of patients with cystic hygroma are chromosomally abnormal; 58% have a karyotype associated with Turner syndrome phenotype; in the remaining 20% autosomal trisomies and various structural abnormalities are present 11 .…”
Section: Discussionmentioning
confidence: 99%
“…These lesions are present at birth and have a progressive clinical course. The incidence of LMs is evidenced in about 1 to 6000 to 1 to 16,000 live births, with a frequency of hospitalization -3 cases per 100,000 [4,5]. LMs near the principal lymphatic chains in the neck region are formed when a primordial lymph sac loses or fails to re-establish communication with the central veins (jugular and subclavian) from which it arises [1].…”
Section: Introductionmentioning
confidence: 99%