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作 者:Ruiz-De-Casas A. Carrizosa-Esquivel A. Herrera-Saval A. 罗素菊
机构地区:[1]Department of Dermatology, Virgen Macarena University Hospital, Seville, Spain Dr.
出 处:《世界核心医学期刊文摘(皮肤病学分册)》2006年第6期35-35,共1页Digest of the World Core Medical JOurnals:Dermatology
摘 要:Sézary syndrome (SS) is a leukaemic variant of cutaneous T-cell lymphoma (CTCL). We report a patient with SS who developed granulomatous lesions. These lesions broke out during treatment with bexarotene when the disease had appeared to stabilize. After a partial clinical remission the disease showed rapid progression and finally led to the patient’s death. This contradicts the initial assessment, which considered the granulomatous inflammation as a good prognostic factor in CTCL.Sézary syndrome (SS) is a leukaemic variant of cutaneous T-cell lymphoma (CTCL). We report a patient with SS who developed granulomatous lesions. These lesions broke out during treatment with bexarotene when the disease had appeared to stabilize. After a partial clinical remission the disease showed rapid progression and finally led to the patient's death. This contradicts the initial assessment, which considered the granulomatous inflammation as a good prognostic factor in CTCL.
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