Yao Yongxue, Mark Lawrence A
Department of Dermatology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Cutis. 2012 Dec;90(6):307-9, 316.
Woringer-Kolopp disease, also known as localized pagetoid reticulosis, is a rare cutaneous lymphoproliferative disorder classified as a solitary variant of mycosis fungoides (MF). Despite the indolent and benign nature of the disease, misdiagnosis and inappropriate treatment may result in years of debilitating symptoms and even loss of function. We present the case of a patient with long-standing Woringer-Kolopp disease that mimicked foot dermatitis. Histopathologic examination demonstrated epidermotropic infiltration of atypical lymphocytes that were CD3+ CD4- CD8-. The patient was successfully treated with topical keratolytics and bexarotene gel 1% with minimal residual lesions after 8 years of follow-up. We discuss the characteristics of this rare disease in contrast with localized MF as well as more aggressive forms of epidermotropic T-cell lymphoma.
沃林格-科洛普病,又称局限性蕈样网状细胞增生症,是一种罕见的皮肤淋巴细胞增殖性疾病,被归类为蕈样肉芽肿(MF)的孤立性变种。尽管该疾病具有惰性和良性性质,但误诊和不恰当的治疗可能导致多年的衰弱症状,甚至功能丧失。我们报告一例长期患有类似足部皮炎的沃林格-科洛普病患者。组织病理学检查显示非典型淋巴细胞呈亲表皮浸润,这些细胞CD3 + CD4 - CD8 -。患者经外用角质溶解剂和1%贝沙罗汀凝胶成功治疗,随访8年后残留病变极少。我们将这种罕见疾病的特征与局限性MF以及更具侵袭性的亲表皮性T细胞淋巴瘤进行了讨论。