Department of Nephrology, Albert Schweitzer hospital, Dordrecht, The Netherlands.
Pathol Int. 2011 Nov;61(11):672-6. doi: 10.1111/j.1440-1827.2011.02718.x. Epub 2011 Sep 23.
We present a case of atypical idiopathic retroperitoneal fibrosis (iRPF) presenting as a large pelvic tumor, for which it proved difficult to exclude T-cell malignant lymphoma. Histopathological examination of biopsy material showed collagenous tissue and fat with an exuberant and predominant T-cell infiltrate, largely consisting of CD4(+) cells expressing the IL-2 receptor-α chain (CD25). Focal plasma cells were negative for the immunoglobulin G4 (IgG4) isotype. T-cell receptor gene rearrangement (TRGR) pattern showed a Gaussian distribution, in keeping with a polyclonal T-cell population. Awareness of the sometimes exuberant and predominant T-cell infiltrate in iRPF should lead to earlier consideration of this disorder. This is particularly the case where there is an atypically localized and/or extensive mass, for which early exclusion of monoclonality with TRGR may provide helpful. Immunohistochemical findings suggest that CD4(+) CD25(+) cells, which are part of a naturally occurring population of regulatory T-cells, may be involved in the pathogenesis of iRPF.
我们报告一例表现为巨大盆腔肿瘤的非典型特发性腹膜后纤维化(iRPF)病例,其难以排除 T 细胞恶性淋巴瘤。活检材料的组织病理学检查显示胶原组织和脂肪,其中有丰富且占主导地位的 T 细胞浸润,主要由表达白细胞介素 2 受体-α 链(CD25)的 CD4(+)细胞组成。局部浆细胞对免疫球蛋白 G4(IgG4)同型呈阴性。T 细胞受体基因重排(TRGR)模式呈高斯分布,符合多克隆 T 细胞群。认识到 iRPF 中有时会出现丰富且占主导地位的 T 细胞浸润,应更早考虑这种疾病。在存在非典型局部和/或广泛肿块的情况下尤其如此,早期通过 TRGR 排除单克隆性可能会有所帮助。免疫组化结果表明,CD4(+)CD25(+)细胞是调节性 T 细胞自然存在的一部分,可能参与 iRPF 的发病机制。