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
  • [1] Enzyme replacement therapy of fabry disease
    Joe T. R. Clarke
    R. Mark Iwanochko
    Molecular Neurobiology, 2005, 32 : 43 - 50
  • [2] Enzyme replacement therapy of Fabry disease
    Clarke, JTR
    Iwanochko, RM
    MOLECULAR NEUROBIOLOGY, 2005, 32 (01) : 43 - 50
  • [3] Enzyme replacement therapy in Fabry disease
    Grundmann, F.
    Benzing, T.
    Kurschat, C.
    NEPHROLOGE, 2015, 10 (03): : 207 - 213
  • [4] Fabry disease:: enzyme replacement therapy
    Bongiorno, MR
    Pistone, G
    Aricò, M
    JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2003, 17 (06) : 676 - 679
  • [5] Enzyme replacement therapy in an adolescent with Fabry disease
    Sabine Illsinger
    Thomas Luecke
    Hendrik Langen
    Anibh M. Das
    European Journal of Pediatrics, 2003, 162 : 522 - 523
  • [6] Utility of enzyme replacement therapy in Fabry disease
    Manuel Politei, Juan
    Dubroysky, Alberto
    MEDICINA CLINICA, 2010, 134 (09): : 402 - 405
  • [7] The use of agalsidase alfa enzyme replacement therapy in the treatment of Fabry disease
    Morell, Chantal F.
    Clarke, Joe T. R.
    EXPERT OPINION ON BIOLOGICAL THERAPY, 2009, 9 (05) : 631 - 639
  • [8] Discontinuation of enzyme replacement therapy in Fabry disease in the Dutch cohort
    Arends, Maarten
    Linthorst, Gabor E.
    Hollak, Carla E.
    Biegstraaten, Marieke
    MOLECULAR GENETICS AND METABOLISM, 2016, 117 (02) : 194 - 198
  • [9] Manifestation of Fabry disease in a heterozygous female patient: new perspectives arising from enzyme replacement therapy
    Jansen, T.
    Brokalaki, E.
    Hillen, U.
    Hentschke, M.
    Grabbe, S.
    DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 2006, 131 (28-29) : 1590 - 1593
  • [10] Clinical benefit of enzyme replacement therapy in Fabry disease
    Breunig, F
    Weidemann, F
    Strotmann, J
    Knoll, A
    Wanner, C
    KIDNEY INTERNATIONAL, 2006, 69 (07) : 1216 - 1221