Katsura Yukitaka, Suzukawa Kazumi, Kojima Hiroshi, Yoshida Chikashi, Shimizu Seiichi, Mukai Harumi, Hasegawa Yuichi, Imagawa Shigehiko, Mori Naoyoshi, Nagasawa Toshiro
Division of Hematology, Institute of Clinical Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
Int J Hematol. 2003 Apr;77(3):282-5. doi: 10.1007/BF02983787.
The case of a 49-year-old man with peripheral T-cell lymphoma arising in Behcet disease (BD) is reported. A diagnosis of incomplete BD was made, and the patient was treated with immunosuppressive agents for 9 months. A left perirenal mass emerged, and a computed tomography-guided needle biopsy of the tumor revealed the infiltration of small- and medium-sized lymphoma cells. The cells were positive for CD3, CD8, CD45RO, CD43, granzyme B, and T-cell intracellular antigen-1. A diagnosis of non-Hodgkin's lymphoma (diffuse medium, T-cell) was made. A left orbital mass also appeared. Standard combination chemotherapy diminished the perirenal and orbital lesions. Lymphoma cell infiltration in the esophagus was detected after chemotherapy, and the patient died of massive bleeding from the gastrointestinal tract. Non-Hodgkin's lymphoma is rarely associated with BD, and only 7 cases have been reported in the literature. We have summarized the published case reports of malignant lymphoma arising in BD. To our knowledge, this case report is the first to describe cytotoxic T-cell lymphoma arising in Behçet disease.
报告了1例白塞病(BD)合并外周T细胞淋巴瘤的49岁男性病例。该患者被诊断为不完全性BD,并接受了9个月的免疫抑制剂治疗。之后出现左肾周肿块,计算机断层扫描引导下的肿瘤穿刺活检显示有中小淋巴瘤细胞浸润。这些细胞CD3、CD8、CD45RO、CD43、颗粒酶B和T细胞胞内抗原-1呈阳性。诊断为非霍奇金淋巴瘤(弥漫性中等大小,T细胞型)。同时还出现了左眼眶肿块。标准联合化疗使肾周和眼眶病变缩小。化疗后检测到食管有淋巴瘤细胞浸润,患者死于胃肠道大出血。非霍奇金淋巴瘤很少与BD相关,文献中仅报道过7例。我们总结了已发表的BD合并恶性淋巴瘤的病例报告。据我们所知,本病例报告是首例描述白塞病合并细胞毒性T细胞淋巴瘤的报告。