Chronic lymphangiectasis in Turner's syndrome.
Identifieur interne : 009B75 ( Ncbi/Merge ); précédent : 009B74; suivant : 009B76Chronic lymphangiectasis in Turner's syndrome.
Auteurs : H D Perry ; A J CossariSource :
- The British Journal of Ophthalmology [ 0007-1161 ] ; 1986.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Conjonctive, Lymphoedème, Système lymphatique, Tissu conjonctif.
- Enfant d'âge préscolaire, Femelle, Humains, Lymphangiectasie, Lymphoedème, Syndrome de Turner.
English descriptors
- KwdEn :
- MESH :
- complications : Lymphangiectasis, Lymphedema, Turner Syndrome.
- congenital : Lymphedema.
- pathology : Conjunctiva, Connective Tissue, Lymphatic System, Lymphedema.
- Child, Preschool, Female, Humans.
Abstract
A 3 1/2-year-old female presented with Turner's syndrome and Nonne-Milroy-Meige disease. Ocular findings included strabismus and bilateral chemosis which was unchanging and persisted throughout the four years the patient was followed up. Histopathological findings included diffuse lymphangiectasia and dense connective tissue surrounding the dilated lymph channels. Although the association between congenital lymphoedema and Turner's syndrome is common, the lymphoedema usually disappears by the first year of life. The persistence of the lymphoedema beyond this age is rare, as is the presence of the persistent chemosis. This report represents the first histopathological documentation of congenital lymphangiectasis in association with Turner's syndrome.
Url:
PubMed: 3964640
PubMed Central: 1041022
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PMC:1041022Le document en format XML
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<front><div type="abstract" xml:lang="en">A 3 1/2-year-old female presented with Turner's syndrome and Nonne-Milroy-Meige disease. Ocular findings included strabismus and bilateral chemosis which was unchanging and persisted throughout the four years the patient was followed up. Histopathological findings included diffuse lymphangiectasia and dense connective tissue surrounding the dilated lymph channels. Although the association between congenital lymphoedema and Turner's syndrome is common, the lymphoedema usually disappears by the first year of life. The persistence of the lymphoedema beyond this age is rare, as is the presence of the persistent chemosis. This report represents the first histopathological documentation of congenital lymphangiectasis in association with Turner's syndrome.</div>
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