A CASE REPORT: TRANSFORMATION OF ERYTHRODERMIC PSORIASIS TO CUTANEOUS T-CELL LYMPHOMA

Ismiralda Oke Putranti, Amelia B Rahardjo, Citra Primanita, Lilik Karsono, Arundito Widikusumo
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Abstract

Background: Erythrodermic psoriasis (EP) is a severe type of psoriasis, a chronic inflammatory disease characterized by general erythematous condition with thick scale all around the body. The treatment of EP consists systemic medications like cyclosporine or methotrexate and biologic agents, which lately suggested related to the development of cutaneous T-cell lymphoma (CTCL) in severe psoriasis patients. Case Report: A 45-year old, Javanese male was diagnosed previously with EP that transformed to CTCL. His previous history, he was histologically confirmed as psoriasis vulgaris since 2014 and was treated regularly with methotrexate. After 5 years, he gradually suffered several episodes of erythrodermic condition and was diagnosed with erythrodermic psoriasis with unusual pruritic hyperkeratotic plaques and ulcers on his trunks without any general lymph nodes enlargement. Peripheral blood smear showed Sezary cell and histopathology result confirmed CTCL. He was treated with combination of radiotherapy, phototherapy and topical regiments with a good result and acceptable. Discussion: Several studies suggested that severe psoriasis had increased the susceptibility of CTCL, especially with the use of cyclosporine, methotrexate or biologic agents as the treatment. In this case, methotrexate might play role in the development of CTCL or enhanced the transformation of EP to CTCL. Combination of localized radiation therapy, NBUVB and topical therapy gave a quiet good result for the skin condition and increased patient’s quality of life. Conclusion: Erythrodermic psoriasis might transform or develop to CTCL which in this case was probably related to the use of methotrexate.    
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红皮病型银屑病转化为皮肤t细胞淋巴瘤1例报告
背景:红皮病型牛皮癣(EP)是一种严重类型的牛皮癣,是一种慢性炎症性疾病,其特征是全身厚鳞的全身红斑状态。EP的治疗包括全身药物,如环孢素或甲氨蝶呤和生物制剂,最近被认为与严重银屑病患者皮肤t细胞淋巴瘤(CTCL)的发展有关。病例报告:一名45岁的爪哇男性先前被诊断为EP转化为CTCL。既往病史:2014年起组织学确诊为寻常型银屑病,定期接受甲氨蝶呤治疗。5年后,他逐渐出现几次红皮病发作,并被诊断为红皮病性牛皮癣,躯干出现异常瘙痒性角化过度斑块和溃疡,没有任何淋巴结肿大。外周血涂片示上皮细胞,组织病理证实为CTCL。经放疗、光疗及局部用药治疗,效果良好,可接受。讨论:一些研究表明,严重的银屑病增加了CTCL的易感性,特别是使用环孢素、甲氨蝶呤或生物制剂作为治疗。在这种情况下,甲氨蝶呤可能在CTCL的发展中起作用或增强EP向CTCL的转化。局部放疗、NBUVB联合局部治疗对皮肤状况有较好的改善效果,提高了患者的生活质量。结论:红皮病型银屑病可能转化或发展为CTCL,可能与甲氨蝶呤的使用有关。
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