Schleyer V, Meyer S, Landthaler M, Szeimies R-M
Klinik und Poliklinik für Dermatologie der Universität Regensburg, Regensburg.
Hautarzt. 2004 Jul;55(7):658-62. doi: 10.1007/s00105-004-0733-4.
Mastocytoses are a heterogenous group of diseases characterized by proliferation and accumulation of mast cells in the skin and other organs. They are subdivided into cutaneous mastocytoses; systemic forms, which may appear with or without skin lesions; mast cell sarcomas and extracutaneous, localized, benign mastocytomas. Systemic mastocytoses apart from the skin mainly involve bone marrow, gastrointestinal tract, bones, lymph nodes, spleen and liver. Whereas indolent forms of systemic mastocytosis are mainly treated with antihistamines, glucocorticosteroids and PUVA therapy, the more aggressive forms, including mast cell leukemia, often require cytostatic chemotherapy. A 53-year old patient with beginning "smoldering systemic mastocytosis" failed to respond to high-dose systemic glucocorticosteroids and interferon-alpha. Treatment with cladribine led to an impressive improvement of skin lesions, a significant decrease in tryptase serum levels and stabilization of bone marrow infiltrates.
肥大细胞增多症是一组异质性疾病,其特征是肥大细胞在皮肤和其他器官中增殖和积聚。它们可细分为皮肤肥大细胞增多症;系统性形式,可伴有或不伴有皮肤病变;肥大细胞肉瘤以及皮肤外局限性良性肥大细胞瘤。除皮肤外,系统性肥大细胞增多症主要累及骨髓、胃肠道、骨骼、淋巴结、脾脏和肝脏。惰性系统性肥大细胞增多症主要用抗组胺药、糖皮质激素和补骨脂素紫外线疗法治疗,而侵袭性更强的形式,包括肥大细胞白血病,通常需要细胞毒性化疗。一名53岁初发“冒烟型系统性肥大细胞增多症”患者对高剂量系统性糖皮质激素和α干扰素治疗无效。用克拉屈滨治疗使皮肤病变显著改善,血清类胰蛋白酶水平显著降低,骨髓浸润稳定。