Kojima Motohiro, Sipos Bence, Klapper Wolfram, Frahm Olaf, Knuth Hans-Christian, Yanagisawa Akio, Zamboni Giuseppe, Morohoshi Toshio, Klöppel Günter
Department of Pathology, University of Kiel, Germany.
Am J Surg Pathol. 2007 Apr;31(4):521-8. doi: 10.1097/01.pas.0000213390.55536.47.
Autoimmune pancreatitis (AIP) is a newly recognized disease. The presence of IgG4 positive plasma cells is thought to be of diagnostic help. In a surgical series of chronic pancreatitis cases, we determined the relative frequency of AIP before and after 1990, analyzed the diagnostic significance of IgG4 expression and examined the presence of oligoclonal T or B-cell populations. The histopathology of 202 surgical specimens of chronic pancreatitis removed between 1975 and 2004 was reviewed and 2 groups were distinguished, 1 of AIP cases and the other of nonautoimmune chronic pancreatitis (non-AIP CP). The intensity of infiltration of pancreatic tissue by IgG4 positive plasma cells and other immune cells was studied immunohistochemically. Finally, T and B-cell clonality was tested by polymerase chain reaction-based analysis. Except for 1 case in 1978, all cases of AIP were observed after 1990. IgG4 positive plasma cells were detected in 72.5% of AIP cases and in 63.1% of non-AIP CP cases. More than 20 cells per high power field were only seen in AIP (sensitivity 43%, specificity 100%). This finding was associated with higher age and grade. Polyclonal T and B-cell populations were found in both AIP and non-AIP CP except for 1 AIP case showing an oligoclonal IgGH-FR3 gene rearrangement. AIP seems to have increased considerably in frequency in the last 2 decades. High density infiltrates of IgG4 positive plasma cells are diagnostic for AIP, but are seen in less than half of the cases. T or B-cell oligoclonality could not be established as a feature of AIP.
自身免疫性胰腺炎(AIP)是一种新发现的疾病。IgG4阳性浆细胞的存在被认为有助于诊断。在一组慢性胰腺炎手术病例中,我们确定了1990年前后AIP的相对发病率,分析了IgG4表达的诊断意义,并检测了寡克隆T或B细胞群体的存在情况。回顾了1975年至2004年间切除的202例慢性胰腺炎手术标本的组织病理学,区分出两组,一组为AIP病例,另一组为非自身免疫性慢性胰腺炎(非AIP CP)病例。采用免疫组织化学方法研究了IgG4阳性浆细胞和其他免疫细胞对胰腺组织的浸润强度。最后,通过基于聚合酶链反应的分析检测T和B细胞的克隆性。除1978年的1例病例外,所有AIP病例均在1990年后被观察到。72.5%的AIP病例和63.1%的非AIP CP病例检测到IgG4阳性浆细胞。每高倍视野超过20个细胞仅在AIP中可见(敏感性43%,特异性100%)。这一发现与较高的年龄和分级相关。除1例AIP病例显示寡克隆IgGH-FR3基因重排外,AIP和非AIP CP中均发现多克隆T和B细胞群体。在过去20年中,AIP的发病率似乎有了显著增加。IgG4阳性浆细胞的高密度浸润对AIP具有诊断意义,但仅在不到一半的病例中可见。T或B细胞寡克隆性不能作为AIP的一个特征来确定。