Variable clinical presentation in primary lymphoedema: report of two cases

被引:3
|
作者
Ozyurt, Abdullah [1 ]
Sevinc, Eylem [2 ]
Baykan, Ali [1 ]
Arslan, Duran [2 ]
Argun, Mustafa [1 ]
Pamukcu, Ozge [1 ]
Uzum, Kazim [1 ]
机构
[1] Erciyes Univ, Fac Med, Div Pediat Cardiol, TR-38039 Kayseri, Turkey
[2] Erciyes Univ, Fac Med, Div Pediat Gastroenterol, TR-38039 Kayseri, Turkey
关键词
ascites; Hennekam syndrome; octreotide; primary lymphoedema; HENNEKAM-SYNDROME; MENTAL-RETARDATION; LYMPHANGIECTASIA;
D O I
10.1097/MCD.0000000000000036
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Lymphoedema is a condition of localized fluid retention and tissue swelling caused by a compromised lymphatic system. Lymphoedema may be primary or secondary and can be inherited. Primary lymphoedema (primary lymphatic dysplasia) is a chronic oedema caused by a developmental abnormality of the lymphatic system. Primary lymphoedema most commonly affects the lower limbs, but other body parts can also be affected. It can be associated with some specific syndromes (i.e. Hennekam syndrome) and genetic disorders. In this article, we report on two patients with congenital multisegmental lymphoedema and Hennekam syndrome, both primary lymphoedemas. (C) 2014 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:83 / 87
页数:5
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