Handfield-Jones S E, Smith N P, Breathnach S M
St John's Dermatology Centre, St Thomas' Hospital, London, UK.
Clin Exp Dermatol. 1992 Sep;17(5):374-5. doi: 10.1111/j.1365-2230.1992.tb00238.x.
We report the case of a 25-year-old Jamaican woman with hypopigmented mycosis fungoides. She first developed a hypopigmented patch on her arm at the age of 11 years. Further lesions developed on the trunk and limbs over a period of 10 years. The lesions were completely impalpable. Skin biopsy showed an infiltrate of atypical lymphocytes, some with cerebriform nuclei, suggesting a diagnosis of mycosis fungoides. The lesions cleared with PUVA therapy.
我们报告一例25岁患有色素减退性蕈样肉芽肿的牙买加女性病例。她11岁时首次在手臂上出现色素减退斑。在10年的时间里,躯干和四肢又出现了更多皮损。这些皮损完全触不到。皮肤活检显示非典型淋巴细胞浸润,部分细胞有脑回状核,提示诊断为蕈样肉芽肿。皮损经补骨脂素加长波紫外线(PUVA)疗法后消退。