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皮肤假性淋巴瘤:一例免疫组织化学研究病例报告

Cutaneous pseudolymphoma: a case report with an immunohistochemical study.

作者信息

Terada Tadashi

机构信息

Department of Pathology, Shizuoka City Shimizu Hospital, Shizuoka, Japan.

出版信息

Int J Clin Exp Pathol. 2013 Apr 15;6(5):966-72. Print 2013.

Abstract

Cutaneous pseudolymphoma (C-PSL) is defined as reactive polyclonal benign lymphoproliferative process predominantly composed of either B-cells or T-cells, localized or disseminated. It heals spontaneously after cessation of the causative factor (e.g. drugs) or after non-aggressive treatment. The author herein presents a case of C-PSL with an immunohistochemical study. A 78-year-old man consulted our hospital because of slightly itching skin swelling on the arm. He denied insect bite and traumatic injury. His usual intake drugs were drugs of hypertension, hyperlipidemia, diabetes mellitus, and emotional disorders. Physical examination showed mildly erosive swelling of the am. The lesion measured 1 x 1 x 0.2 cm. Biopsy of the lesion was taken, and it revealed excessive proliferation of small lymphoid cells. The lymphoid cells lacked apparent atypical features and appeared matures. Lymphoblastic cells with nucleoli were scattered. Nodular structures were also seen in the lower dermis. Immunohistochemically, the lymphoid cells were positive for vimentin, CD3, CD4, CD5, CD8, CD10, CD15, CD20, CD23, CD30, CD43, CD38, CD138, CD45RO, CD79α, bcl-2, bcl-6, κ-chain, λ-chain, and Ki-67 (labeling index=7%). No light chain restriction is seen. The lymphoblastic cells were positively labeled for CD15 and CD30. Plasma cells positive for CD38, CK79α and CD138 were seen in a significant amounts. They were negative for cytokeratin (CK) CAM5.2, CKAE1/3, CK34BE12, CK5/6, CK7, CK8, CK18, CK19, CK20, EMA, CEA, CD56, CD57, p53, KIT, PDGFRA, and cyclin D1. Because the constituent cells were both B-cells including plasm cells and T-cells, no light-chain restriction was seen, and no histological atypia was seen, a diagnosis of cutaneous pseudolymphoma was made. The low Ki-67 labeling and negative p53 also suggested the diagnosis. The lesion slightly reduced in size (from 1 cm to 0.7 cm), the causative agent was still unknown 11 months after the biopsy.

摘要

皮肤假性淋巴瘤(C-PSL)被定义为一种反应性多克隆良性淋巴细胞增殖过程,主要由B细胞或T细胞组成,可局限或播散。在致病因素(如药物)停止作用后或经过非侵袭性治疗后可自行愈合。本文作者报告一例皮肤假性淋巴瘤病例并进行了免疫组织化学研究。一名78岁男性因手臂皮肤轻度瘙痒性肿胀前来我院就诊。他否认有昆虫叮咬和外伤史。他平时服用的药物有治疗高血压、高脂血症、糖尿病和情绪障碍的药物。体格检查显示手臂有轻度糜烂性肿胀。病变大小为1×1×0.2cm。对病变进行活检,结果显示小淋巴细胞过度增殖。这些淋巴细胞缺乏明显的非典型特征,看起来成熟。可见有核仁的淋巴母细胞散在分布。在真皮深层也可见结节状结构。免疫组织化学检查显示,淋巴细胞波形蛋白、CD3、CD4、CD5、CD8、CD10、CD15、CD20、CD23、CD30、CD43、CD38、CD138、CD45RO、CD79α、bcl-2、bcl-6、κ链、λ链和Ki-67呈阳性(标记指数=7%)。未见轻链限制。淋巴母细胞CD15和CD30呈阳性标记。可见大量CD38、CK79α和CD138阳性的浆细胞。它们细胞角蛋白(CK)CAM5.2、CKAE1/3、CK34BE12、CK5/6、CK7、CK8、CK18、CK19、CK20、EMA、CEA、CD56、CD57、p53、KIT、PDGFRA和细胞周期蛋白D1呈阴性。由于组成细胞既有包括浆细胞在内的B细胞,也有T细胞,未见轻链限制,也未见组织学非典型性,故诊断为皮肤假性淋巴瘤。低Ki-67标记和p53阴性也支持该诊断。病变大小略有缩小(从1cm缩小至0.7cm),活检11个月后仍未明确致病因素。

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