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血管中心的生长模式在组织学上表现为血管炎的非典型性低分化皮肤T淋巴细胞瘤
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作者 Laetsch B Hofbauer G +2 位作者 kempf w R. Dum-mer 惠海英 《世界核心医学期刊文摘(皮肤病学分册)》 2005年第10期57-58,共2页
We report the case of a 41-year-old patient with an aggressive cutaneous T-cell lymphoma (CTCL) initially presenting on histology as lymphocytic vasculitis. On repeated histological examination and by molecular biolog... We report the case of a 41-year-old patient with an aggressive cutaneous T-cell lymphoma (CTCL) initially presenting on histology as lymphocytic vasculitis. On repeated histological examination and by molecular biology work-up, the diagnosis of an unclassifiable CTCL could eventually be established. This atypical poorly differentiated lymphoma was of a CD4+CD8-CD56-phenotype and followed an unfavourable course. The patient died despite chemoand immunotherapy 7 months after the first consideration of lymphoma as diagnosis. 展开更多
关键词 淋巴细胞瘤 血管炎 非典型性 生长模式 淋巴瘤患者 淋巴细胞性 免疫治疗 预后差 弥漫性
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