Wagner G, Bartsch S, Rose C, Sachse M M
Klinik für Dermatologie, Allergologie und Phlebologie, Klinikum Bremerhaven Reinkenheide, Postbrookstr. 103, 27574, Bremerhaven, Deutschland.
Hautarzt. 2012 Dec;63(12):965-8. doi: 10.1007/s00105-012-2436-6.
A 39-year-old man presented with an annular clearly palpable erythema on the décolleté. Based on clinical and histopathological findings, palpable migratory arciform erythema was diagnosed. This skin condition is classified as a rare type of T-cell pseudolymphoma. It is still a matter of debate whether palpable migratory arciform erythema is a specific entity or a clinical variant of lymphocytic infiltration of the skin (Jessner-Kanof). Topical corticosteroids or oral antibiotics are generally used. In our patient, UV-A1 therapy led to a complete regression of the lesions.
一名39岁男性患者，其胸部出现了一个可清晰触及的环状红斑。根据临床和组织病理学检查结果，诊断为可触及的游走性弧形红斑。这种皮肤疾病被归类为一种罕见的T细胞假性淋巴瘤。可触及的游走性弧形红斑究竟是一种特定的疾病实体还是皮肤淋巴细胞浸润（杰斯纳 - 卡诺夫病）的临床变体，目前仍存在争议。通常使用局部皮质类固醇或口服抗生素进行治疗。在我们的患者中，UV - A1疗法使皮损完全消退。
