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复杂形式的乳糜泻是隐匿性T细胞淋巴瘤吗?

Are complicated forms of celiac disease cryptic T-cell lymphomas?

作者信息

Carbonnel F, Grollet-Bioul L, Brouet J C, Teilhac M F, Cosnes J, Angonin R, Deschaseaux M, Châtelet F P, Gendre J P, Sigaux F

机构信息

Service de Gastroentérologie et Nutrition and the Laboratoire d'Anatomopathologie, Hôpital Rothschild, Paris, France.

出版信息

Blood. 1998 Nov 15;92(10):3879-86.

PMID:9808581
Abstract

We assessed the clonality of duodenal mucosal T cells in patients with celiac disease and controls. Fifteen adult patients were studied. Four patients had a complicated celiac disease, 3 did not respond to a gluten-free diet, and 2 had an ulcerative jejunitis (including 1 patient with nonresponsive celiac disease). Seven patients had an untreated celiac disease responsive to a gluten-free diet. Histological examination of duodenal biopsies of these 11 patients showed benign-appearing celiac disease without evidence of lymphoma. Four patients with nonulcer dyspepsia and normal duodenal biopsies served as controls. TCRgamma gene rearrangements were analyzed by multiplex polymerase chain reaction on DNA extracted from duodenal biopsies. Major clonal rearrangements of the T-cell receptor were found in 4 cases, all with complicated celiac disease. Monoclonality was confirmed by DNA sequencing of the junctional region in 3 cases and by hybridization with clone-specific oligoprobes. Patients with celiac disease responsive to gluten-free diet had mainly a polyclonal pattern, with 1 of them having an oligoclonal rearrangement. An oligoclonal pattern was also observed in 2 control patients. Three patients with complicated celiac disease evolved to T-cell lymphoma with liver (n = 2) or bone marrow (n = 1) invasion. Identical clones were found in the enteropathic duodenojejunum and peripheral blood in the patient with large-cell lymphoma with bone marrow invasion. This study suggests that complicated celiac disease is a cryptic T-cell lymphoma.

摘要

我们评估了乳糜泻患者和对照者十二指肠黏膜T细胞的克隆性。研究了15名成年患者。4例患者患有复杂型乳糜泻,3例对无麸质饮食无反应,2例患有溃疡性空肠炎(包括1例对无麸质饮食无反应的乳糜泻患者)。7例患者患有未经治疗但对无麸质饮食有反应的乳糜泻。对这11例患者十二指肠活检组织进行组织学检查,结果显示为良性乳糜泻,无淋巴瘤证据。4例非溃疡性消化不良且十二指肠活检正常的患者作为对照。通过多重聚合酶链反应对从十二指肠活检组织中提取的DNA进行TCRγ基因重排分析。在4例患者中发现了T细胞受体的主要克隆重排,所有这些患者均患有复杂型乳糜泻。3例通过连接区DNA测序以及与克隆特异性寡核苷酸探针杂交证实为单克隆性。对无麸质饮食有反应的乳糜泻患者主要为多克隆模式,但其中1例有寡克隆重排。2例对照患者也观察到寡克隆模式。3例复杂型乳糜泻患者发展为T细胞淋巴瘤,伴有肝脏(n = 2)或骨髓(n = 1)浸润。在患有骨髓浸润的大细胞淋巴瘤患者的病变十二指肠空肠和外周血中发现了相同的克隆。这项研究表明,复杂型乳糜泻是一种隐匿性T细胞淋巴瘤。

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