Bergström Anna, Rollman Ola, Emtestam Lennart, Mattson Mattias, Hägglund Hans, Nilsson Gunnar, Karlsson Maria
Hudkliniken - Akademiska sjukhuset Uppsala, Sweden Hudkliniken - Akadmiska sjukhuset Uppsala, Sweden.
Inst med vetenskaper - Uppsala Universitet Uppsala, Sweden Inst med vetenskaper - Uppsala Universitet Uppsala, Sweden.
Lakartidningen. 2018 Oct 22;115:FASY.
Mastocytosis is a rare and multifaceted disease group characterized by mast cell accumulation in the skin and/or internal organs. In its most common form solitary or widespread, often itchy, red-brown skin lesions appear in childhood or during adulthood (cutaneous mastocytosis). The skin lesions are not always easy to recognize by medical professionals; hence, a correct diagnosis is often delayed. In children, the lesions tend to resolve before puberty, whereas most post-adolescent patients experience a chronic course combined with extra-cutaneous mast cell infiltration (systemic mastocytosis). Therefore, adult patients with cutaneous mastocytosis should be examined for signs of systemic involvement. This article describes the symptoms and signs in cutaneous mastocytosis, and provides guidelines based on international consensus documents. In addition, a newly updated classification of different forms of cutaneous mastocytosis is given.
肥大细胞增多症是一组罕见且多方面的疾病,其特征是肥大细胞在皮肤和/或内脏器官中积聚。其最常见的形式为孤立性或广泛性,通常伴有瘙痒的红棕色皮肤病变出现在儿童期或成年期(皮肤肥大细胞增多症)。医学专业人员并不总是容易识别这些皮肤病变;因此,正确诊断往往会延迟。在儿童中,病变往往在青春期前消退,而大多数青春期后的患者会经历慢性病程并伴有皮肤外肥大细胞浸润(系统性肥大细胞增多症)。因此,患有皮肤肥大细胞增多症的成年患者应检查是否有系统性受累的迹象。本文描述了皮肤肥大细胞增多症的症状和体征,并根据国际共识文件提供了指导方针。此外,还给出了不同形式皮肤肥大细胞增多症的最新分类。