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
相关论文
共 13 条
  • [1] Further delineation of Hennekam syndrome
    Al-Gazali, LI
    Hertecant, J
    Ahmed, R
    Khan, NA
    Padmanabhan, R
    [J]. CLINICAL DYSMORPHOLOGY, 2003, 12 (04) : 227 - 232
  • [2] Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans
    Alders, Marielle
    Hogan, Benjamin M.
    Gjini, Evisa
    Salehi, Faranak
    Al-Gazali, Lihadh
    Hennekam, Eric A.
    Holmberg, Eva E.
    Mannens, Marcel M. A. M.
    Mulder, Margot F.
    Offerhaus, G. Johan A.
    Prescott, Trine E.
    Schroor, Eelco J.
    Verheij, Joke B. G. M.
    Witte, Merlijn
    Zwijnenburg, Petra J.
    Vikkula, Mikka
    Schulte-Merker, Stefan
    Hennekam, Raoul C.
    [J]. NATURE GENETICS, 2009, 41 (12) : 1272 - 1274
  • [3] Angle B, 1997, AM J MED GENET, V71, P211, DOI 10.1002/(SICI)1096-8628(19970808)71:2<211::AID-AJMG17>3.3.CO
  • [4] 2-E
  • [5] Hennekam syndrome presenting as nonimmune hydrops fetalis, congenital chylothorax, and congenital pulmonary lymphangiectasia
    Bellini, C
    Mazzella, M
    Arioni, C
    Campisi, C
    Taddei, G
    Tomà, P
    Boccardo, F
    Hennekam, RC
    Serra, G
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 120A (01): : 92 - 96
  • [6] The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings
    Connell, F. C.
    Gordon, K.
    Brice, G.
    Keeley, V.
    Jeffery, S.
    Mortimer, P. S.
    Mansour, S.
    Ostergaard, P.
    [J]. CLINICAL GENETICS, 2013, 84 (04) : 303 - 314
  • [7] Spectral Endoscopic Imaging The Multiband System for Enhancing the Endoscopic Surface Visualization
    Fedeli, Paolo
    Gasbarrini, Antonio
    Cammarota, Giovanni
    [J]. JOURNAL OF CLINICAL GASTROENTEROLOGY, 2011, 45 (01) : 6 - 15
  • [8] AUTOSOMAL RECESSIVE INTESTINAL LYMPHANGIECTASIA AND LYMPHEDEMA, WITH FACIAL ANOMALIES AND MENTAL-RETARDATION
    HENNEKAM, RCM
    GEERDINK, RA
    HAMEL, BCJ
    HENNEKAM, FAM
    KRAUS, P
    RAMMELOO, JA
    TILLEMANS, AAW
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 34 (04): : 593 - 600
  • [9] Two brothers with Hennekam syndrome and cerebral abnormalities
    Huppke, P
    Christen, HJ
    Sattler, B
    Hanefeld, F
    [J]. CLINICAL DYSMORPHOLOGY, 2000, 9 (01) : 21 - 24
  • [10] Nisli K, 2008, TURK KARDIYOL DERN A, V36, P325