蕈样真菌病
淋巴增殖性病變
医学
免疫抑制
病理
淋巴瘤
CD30
皮肤T细胞淋巴瘤
T细胞
移植
外周T细胞淋巴瘤
人口
T细胞淋巴瘤
免疫学
免疫系统
内科学
环境卫生
作者
Jessica F. Williams,Fabienne Lucas,Ruben D. Carrasco,Scott B. Lovitch,David C. Fisher,Thomas S. Kupper,Sam Sadigh
摘要
Abstract Posttransplantation primary cutaneous T‐cell lymphomas (PT‐CTCL) are a rare complication of sustained immunosuppression in the posttransplant setting. When present, PT‐CTCLs are typically EBV− and exhibit features of mycosis fungoides/Sézary syndrome or CD30+ lymphoproliferative disorders. We present a case of a 75‐year‐old individual who developed skin lesions 30 years after liver transplantation. Pathologic evaluation of the skin biopsy revealed involvement by a clonal, EBV+ T‐cell population of gamma/delta lineage with no evidence of systemic disease. Comprehensive genomic profiling was performed, confirming focal one‐copy loss of 6q23.3, altogether consistent with the extremely rare and unusual diagnosis of primary cutaneous EBV+ extranodal NK/T‐cell lymphoma of gamma/delta T‐cell lineage in the posttransplantation setting.
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