Marton I, Pósfai É, Borbényi Z, Bödör C, Papp G, Demeter J, Korom I, Varga E, Bata-Csörgő Z
2nd Department of Medicine and Cardiology Centre, Medical Faculty, Albert Szent-Györgyi Clinical Centre, University of Szeged, Szeged, Hungary.
Eur Rev Med Pharmacol Sci. 2015;19(9):1607-9.
From a dermatological aspect, it posed a considerable challenge the skin-limited form of mastocytosis, urticaria pigmentosa and indolent systemic mastocytosis (ISM) with cutaneous lesions. Despite the favourable prognosis, lifelong dermatological control is needed, during which the average symptomatic therapy does not always seem adequate. We report here the case of a female ISM patient with recurrent cutaneous symptoms that impaired her quality of life, with a follow-up time of 27 years. During this long follow-up period, the cutaneous lesions could be controlled by antihistamines, leukotriene antagonists, glucocorticoids, local immunosuppressants or local UV radiation for only relatively short periods. Imatinib mesylate was, therefore, introduced in an attempt to control the cutaneous lesions. Tyrosine kinase inhibition is an unusual dermatological therapeutic option. This case illustrates that imatinib mesylate was a good choice with which to achieve a reduction of the skin lesions in this KIT D816V mutation-negative disease: it led to a temporary appreciable improvement of the patient's quality of life.
从皮肤病学角度来看,肥大细胞增多症的皮肤局限性形式、色素性荨麻疹和伴有皮肤损害的惰性系统性肥大细胞增多症(ISM)构成了相当大的挑战。尽管预后良好,但仍需要终身的皮肤病学管理,在此期间,一般的对症治疗似乎并不总是足够的。我们在此报告一例患有复发性皮肤症状且影响其生活质量的女性ISM患者,随访时间为27年。在这一漫长的随访期间,皮肤损害仅在相对较短的时间内可通过抗组胺药、白三烯拮抗剂、糖皮质激素、局部免疫抑制剂或局部紫外线照射得到控制。因此,引入甲磺酸伊马替尼以试图控制皮肤损害。酪氨酸激酶抑制是一种不常见的皮肤病治疗选择。该病例表明,甲磺酸伊马替尼是在这种KIT D816V突变阴性疾病中减少皮肤损害的良好选择:它使患者的生活质量暂时得到明显改善。