Sitthinamsuwan Panitta, Pongpruttipan Tawatchai, Bunyaratavej Sumanas, Karoopongse Ekapan, Kummalue Tanawan, Sukpanichnant Sanya
Department of Pathology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
J Cutan Pathol. 2011 Dec;38(12):1004-8. doi: 10.1111/j.1600-0560.2011.01758.x. Epub 2011 Aug 23.
We report a 51-year-old woman with cutaneous involvement by extranodal NK/T-cell lymphoma (TCL) of the colon that microscopically mimicked mycosis fungoides (MF). She had a history of fever of unknown origin for 2 months and then developed multiple erythematous papules on her trunk and extremities. A skin biopsy revealed superficial infiltration by atypical small to medium-sized lymphocytes with epidermotropism and Pautrier collections. Immunohistochemical studies showed expression of CD3 and TIA-1 with lack of expression (double negative) of CD4 and CD8. Initially, we reported the diagnosis as MF, cytotoxic variant. Thereafter, computerized tomography scan incidentally identified a colonic mass. A colonic biopsy revealed infiltration of atypical lymphoid cells with the same morphology and immunophenotype as those found in the skin. Additionally, CD56 and Epstein-Barr virus-encoded RNA in situ hybridization in both skin and colonic biopsies were diffusely positive. Thus, extranodal NK/TCL was diagnosed. Delta T-cell receptor (TCR) gene rearrangement was documented in the skin biopsy by polyacrylamide gel electrophoresis and fluorescence capillary gel electrophoresis methods. There was no TCR gene rearrangement detected in the colonic biopsy. Unfortunately, the patient died within 2 months of diagnosis.
我们报告了一名51岁女性,其结肠结外NK/T细胞淋巴瘤(TCL)累及皮肤,显微镜下表现类似蕈样肉芽肿(MF)。她有2个月不明原因发热病史,随后躯干和四肢出现多个红斑丘疹。皮肤活检显示非典型中小淋巴细胞呈表皮内浸润及Pautrier微脓肿形成。免疫组化研究显示CD3和TIA-1表达,CD4和CD8表达缺失(双阴性)。最初,我们报告诊断为MF,细胞毒性变异型。此后,计算机断层扫描偶然发现结肠肿物。结肠活检显示非典型淋巴细胞浸润,其形态和免疫表型与皮肤病变相同。此外,皮肤和结肠活检组织中CD56和爱泼斯坦-巴尔病毒编码RNA原位杂交均呈弥漫性阳性。因此,诊断为结外NK/TCL。通过聚丙烯酰胺凝胶电泳和荧光毛细管凝胶电泳方法在皮肤活检中检测到δT细胞受体(TCR)基因重排。结肠活检未检测到TCR基因重排。不幸的是,患者在诊断后2个月内死亡。