Hojo Nobumasa, Yakushijin Yoshihiro, Narumi Hiroshi, Minamoto Yoko, Sakai Ikuya, Takada Kiyonori, Hato Takaaki, Yasukawa Masaki, Fujita Shigeru
First Department of Internal Medicine, Ehime University School of Medicine, Onsen-Gun, Ehime, Japan.
Int J Hematol. 2003 May;77(4):387-90. doi: 10.1007/BF02982649.
A 29-year-old man developed diffuse large B-cell lymphoma in a subpectoral pacemaker pocket that 6 years previously had been created in the chest for a titanium-covered pulse generator. The patient had an 8-cm-diameter dark red tumor with necrotic tissue on a keloidal surgical scar in the left side of the chest. Left axillary lymphadenopathy also was present. Laboratory studies showed an increased level of soluble interleukin 2 receptor and a normal level of lactose dehydrogenase. A biopsy specimen showed a diffuse large B-cell phenotype and monoclonal immunoglobulin H gene rearrangement. A gallium scintigraphy study showed abnormal accumulation in the left chest and left axilla. On the basis of these findings, we diagnosed diffuse large B-cell lymphoma, stage II. The patient received THP-COP chemotherapy (pirarubicin, cyclophosphamide, vincristine, and prednisolone) and radiotherapy, achieved complete remission, and was free of disease for 16 months after treatment. This case suggests that there was a relationship between the development of non-Hodgkin's lymphoma and the presence of chronic inflammation in the pulse generator pocket.
一名29岁男性在胸肌下起搏器囊袋处发生弥漫性大B细胞淋巴瘤,该囊袋于6年前在胸部为置入钛覆盖的脉冲发生器而创建。患者左侧胸部有一个直径8厘米的暗红色肿瘤,位于瘢痕疙瘩样手术瘢痕上,伴有坏死组织。左侧腋窝也有淋巴结肿大。实验室检查显示可溶性白细胞介素2受体水平升高,乳酸脱氢酶水平正常。活检标本显示为弥漫性大B细胞表型及单克隆免疫球蛋白H基因重排。镓闪烁扫描研究显示左胸和左腋窝有异常积聚。基于这些发现,我们诊断为弥漫性大B细胞淋巴瘤,II期。患者接受了THP-COP化疗(吡柔比星、环磷酰胺、长春新碱和泼尼松龙)及放疗,实现完全缓解,治疗后16个月无疾病复发。该病例提示非霍奇金淋巴瘤的发生与脉冲发生器囊袋处慢性炎症的存在之间存在关联。