Metsähonkala Liisa, Valanne Leena, Anttonen Anna-Kaisa
HYKS, konsultaatio ja epilepsiaklinikka, lastenneurologian klinikkaryhmä.
Duodecim. 2013;129(17):1779-87.
Tuberous sclerosis is a polymorphic, dominantly inherited syndrome caused by an inactivating mutation in a tumor suppressor gene. The disease involves benign tumors in several distinct organs such as the skin, kidneys, heart and central nervous system. The tumors interfere with organ function, but only some exhibit a significant tendency to grow. The clinical picture of tuberous sclerosis varies from nearly symptomless to a severe disease. Treatment of growing tumors associated with tuberous sclerosis is changing significantly, since their growth can be suppressed with rapamycin and its derivatives.
结节性硬化症是一种多态性的常染色体显性遗传综合征,由肿瘤抑制基因的失活突变引起。该疾病涉及多个不同器官的良性肿瘤,如皮肤、肾脏、心脏和中枢神经系统。这些肿瘤会干扰器官功能,但只有一些表现出明显的生长倾向。结节性硬化症的临床表现从几乎无症状到严重疾病不等。由于雷帕霉素及其衍生物可以抑制与结节性硬化症相关的生长肿瘤的生长,因此其治疗正在发生显著变化。