Angiokeratomas and treatment with enzyme replacement therapy in a patient with Fabry disease

被引:1
|
作者
Sabovic, Eva Klara Merzel [1 ]
Tansek, Mojca Zerjav [2 ]
Groselj, Urh [2 ]
Dragos, Vlasta [1 ]
机构
[1] Univ Ljubljana, Dept Dermatovenereol, Med Ctr, Ljubljana, Slovenia
[2] Univ Childrens Hosp, Ljubljana Univ Med Ctr, Dept Pediat Endocrinol Diabet & Metab Dis, Ljubljana, Slovenia
来源
ACTA DERMATOVENEROLOGICA ALPINA PANNONICA ET ADRIATICA | 2020年 / 29卷 / 02期
关键词
Fabry disease; angiokeratomas; enzyme replacement therapy; DIAGNOSIS; DISORDER; SKIN;
D O I
10.15570/actaapa.2020.21
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Angiokeratomas are the cutaneous hallmark of Fabry disease. Although it is well established that enzyme replacement therapy (ERT) prevents or slows the progression of disease on target organs in the majority of patients, the long-term effect of ERT on angiokeratomas remains unknown. We present a patient diagnosed with Fabry disease at age 11, with rapid progression of new angiokeratomas in typical regions before beginning treatment with ERT. To date, our patient has been treated with ERT for 10 years. During the treatment period, new angiokeratomas have not arisen nor have existing ones enlarged during puberty, adolescence, and early adulthood. Furthermore, partial regression of the angiokeratomas has occurred in association with regression of left ventricular hypertrophy and anhidrosis. Overall, this case suggests that long-term ERT could stop the progression of angiokeratomas and induce their partial regression but does not produce complete resolution. Importantly, regression of angiokeratomas might be a marker of systemic target-organ efficacy of ERT.
引用
收藏
页码:89 / 91
页数:3
相关论文
共 50 条
  • [21] Enzyme Replacement Therapy in Fabry Disease: Influence on Cardiac Manifestations
    Caballero, L.
    Climent, V.
    Hernandez-Romero, D.
    Quintanilla, M. A.
    de la Morena, G.
    Marin, F.
    CURRENT MEDICINAL CHEMISTRY, 2010, 17 (16) : 1679 - 1689
  • [22] Agalsidase alfa for enzyme-replacement therapy in Fabry disease
    Mehta, Atul
    EXPERT REVIEW OF ENDOCRINOLOGY & METABOLISM, 2010, 5 (05) : 641 - 652
  • [23] FABRY DISEASE: THE IMPORTANCE OF THE, ENZYME REPLACEMENT THERAPY (TRE): TREATING QUICKLY AND EFFICIENTLY
    Politei, Juan
    Schenone, Andrea B.
    Antongiovanni, Norberto
    Cusumano, Ana
    Cabrera, Gustavo
    Szlago, Marina
    REVISTA DE NEFROLOGIA DIALISIS Y TRASPLANTE, 2014, 34 (02): : 82 - 86
  • [24] Effectiveness and safety of enzyme replacement therapy in the treatment of Fabry disease: a Chinese monocentric real-world study
    Liu, Yingjie
    Li, Ying
    Li, Pei
    Zhang, Songyun
    Zhang, Zhiqing
    ORPHANET JOURNAL OF RARE DISEASES, 2024, 19 (01)
  • [25] Fabry disease: recent advances in enzyme replacement therapy
    Germain, DP
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2002, 11 (10) : 1467 - 1476
  • [26] Neuropathy and Fabry disease: pathogenesis and enzyme replacement therapy
    Schiffmann, Raphael
    ACTA NEUROLOGICA BELGICA, 2006, 106 (02) : 61 - 65
  • [27] Enzyme replacement therapy in Fabry disease: clinical implications
    Breunig, F
    Knoll, A
    Wanner, C
    CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2003, 12 (05) : 491 - 495
  • [28] Thyroid function in Fabry disease before and after enzyme replacement therapy
    Faggiano, A.
    Severino, R.
    Ramundo, V.
    Russo, R.
    Vuolo, L.
    Del Prete, M.
    Marciello, F.
    Lombardi, G.
    Cianciaruso, B.
    Colao, A.
    Pisani, A.
    MINERVA ENDOCRINOLOGICA, 2011, 36 (01) : 1 - 5
  • [29] Fabry disease in Spain:: first analysis of the response to enzyme replacement therapy
    Rivera Gallego, Alberto
    Lopez Rodriguez, Monica
    Barbado Hernandez, Francisco Javier
    Barba Romero, Miguel Angel
    Garcia de Lorenzo y Mateos, Abelardo
    Pintos Morell, Guillen
    MEDICINA CLINICA, 2006, 127 (13): : 481 - 484
  • [30] Impact of enzyme replacement therapy and migalastat on disease progression in females with fabry disease
    Lenders, Malte
    Nowak, Albina
    Cybulla, Markus
    Kaufeld, Jessica
    Koehn, Anja Friederike
    Muschol, Nicole Maria
    Kurschat, Christine
    Brand, Eva
    ORPHANET JOURNAL OF RARE DISEASES, 2025, 20 (01)