Vega Francisco, Chang Chung-Che, Schwartz Mary R, Preti Hector Alejandro, Younes Mamoun, Ewton April, Verm Ray, Jaffe Elaine S
Department of Pathology, Baylor College of Medicine, The Methodist Hospital, Houston, TX 77030, USA.
Am J Surg Pathol. 2006 Apr;30(4):539-44. doi: 10.1097/00000478-200604000-00017.
We describe a unique case of atypical natural killer (NK)-cell proliferation likely related to gluten sensitivity, mimicking NK-cell lymphoma. The patient, a 32-year-old man, has had persistent multiple erythematous bull-eye lesions in the stomach, small bowel, and large bowel for 3 years. Histologically, the lesions were well circumscribed and relatively superficial, composed of atypical medium-sized to large-sized lymphocytes with slightly irregular nuclear contours, a dispersed chromatin pattern, and clear cytoplasm. Immunohistochemistry and flow cytometry showed that the cells were NK cells expressing CD56 (aberrantly bright), T-cell intracellular antigen (TIA)-1, cytoplasmic CD3, and CD94, but not surface CD3, with bright aberrant expression of CD7 and a lack of other NK cell-associated markers. Polymerase chain reaction for rearrangement of the T-cell receptor-gamma chain gene showed no evidence of a clonal T-cell population, and in situ hybridization for Epstein-Barr virus encoded RNA was negative. There was no evidence of the involvement of peripheral blood or bone marrow. Although a diagnosis of extranodal NK/T-cell lymphoma was considered because of the atypical morphology and immunophenotypic aberrancy, no chemotherapy was given because of the relatively superficial nature of the infiltrates, lack of significant symptoms, and negativity for Epstein-Barr virus. Two years after initial presentation, the patient was found to have high titers of antigliadin antibodies with no other evidence of celiac disease. After instituting a gluten-free diet, many of the lesions regressed, suggesting that this atypical NK-cell proliferation may be driven by an anomalous immune response. Awareness of this case may prevent pathologists from misdiagnosing similar lesions as NK/T-cell lymphomas. It is as yet unknown whether this process occurs more commonly in patients with gluten sensitivity, or in other settings, and the pathogenesis is as yet undetermined.
我们描述了一例独特的非典型自然杀伤(NK)细胞增殖病例,可能与麸质敏感性有关,酷似NK细胞淋巴瘤。患者为一名32岁男性,胃部、小肠和大肠出现持续的多发性红斑性靶心样损害已3年。组织学上,损害边界清晰且相对表浅,由非典型的中等大小至大淋巴细胞组成,核轮廓略不规则,染色质呈分散状,胞质清亮。免疫组织化学和流式细胞术显示这些细胞为表达CD56(异常明亮)、T细胞胞内抗原(TIA)-1、胞质CD3和CD94的NK细胞,但不表达表面CD3,CD7呈明亮异常表达,且缺乏其他NK细胞相关标志物。T细胞受体γ链基因重排的聚合酶链反应未显示克隆性T细胞群体的证据,爱泼斯坦-巴尔病毒编码RNA的原位杂交为阴性。无外周血或骨髓受累的证据。尽管由于非典型形态和免疫表型异常曾考虑诊断为结外NK/T细胞淋巴瘤,但由于浸润相对表浅、缺乏明显症状且爱泼斯坦-巴尔病毒阴性,未给予化疗。初次就诊两年后,发现患者抗麦醇溶蛋白抗体滴度高,无其他乳糜泻证据。采用无麸质饮食后,许多损害消退,提示这种非典型NK细胞增殖可能由异常免疫反应驱动。认识此病例可防止病理学家将类似损害误诊为NK/T细胞淋巴瘤。目前尚不清楚此过程在麸质敏感性患者或其他情况下是否更常见,其发病机制也尚未确定。