Sepehr Alireza, Mino-Kenudson Mari, Ogawa Fumihiro, Brugge William R, Deshpande Vikram, Lauwers Gregory Y
Department of Pathology, Gastrointestinal Pathology Service, Division of Gastroenterology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
Am J Surg Pathol. 2008 Dec;32(12):1770-9. doi: 10.1097/PAS.0b013e318185490a.
Autoimmune pancreatitis (AIP) shows a unique spectrum of histologic features and commonly presents with an abundant IgG4-positive (IgG4+) plasma cell infiltration. However, differentiating AIP from other mass lesions, particularly pancreatic cancer [invasive ductal carcinoma (IDC)] can be clinically challenging. In this study, we evaluated the validity of IgG4 and IgG immunohistochemistry of ampullary and periampullary tissue for the diagnosis of AIP. Our study group consisted of 14 resected AIP cases with appropriate ampullary sections. Superficial ampullary tissue and "shouldering" duodenal mucosa were evaluated for several histologic variables. Immunohistochemistry for IgG4 and IgG was performed. The number of IgG4 and IgG-positive plasma cells was counted and an IgG4+ to IgG+ plasma cells ratio (IgG4/IgG ratio) was evaluated. A control cohort was composed of IDC (n=30) and chronic pancreatitis (CP) (n=29). Although an overlap was present between the groups, the overall inflammation and number of plasma cells in and around the ampulla was significantly increased in AIP compared with CP and IDC. Furthermore, although there was some overlap in the crude number of IgG4+ plasma cells of the ampullary and duodenal tissue between AIP, IDC, and CP, an IgG4/IgG ratio, especially of the ampulla, seems diagnostically useful in differentiating AIP from other "mass forming" lesions. When a cut-off of 0.10 was applied, the diagnostic sensitivity and specificity of the ampullary IgG4/IgG ratio was 86% and 95%, respectively. In conclusion, evaluation of ampullary histology and IgG4/IgG ratio might be proven beneficial in discriminating AIP from other mass forming pancreatic lesions.
自身免疫性胰腺炎(AIP)具有独特的组织学特征谱,通常表现为大量IgG4阳性(IgG4+)浆细胞浸润。然而,在临床上,将AIP与其他肿块性病变,尤其是胰腺癌[浸润性导管癌(IDC)]区分开来具有挑战性。在本研究中,我们评估了壶腹和壶腹周围组织的IgG4和IgG免疫组化对AIP诊断的有效性。我们的研究组由14例切除的AIP病例组成,这些病例有合适的壶腹切片。对壶腹浅表组织和“肩部”十二指肠黏膜进行了几个组织学变量的评估。进行了IgG4和IgG的免疫组化。计数IgG4和IgG阳性浆细胞的数量,并评估IgG4+与IgG+浆细胞的比例(IgG4/IgG比例)。对照组由IDC(n = 30)和慢性胰腺炎(CP)(n = 29)组成。尽管各组之间存在重叠,但与CP和IDC相比,AIP中壶腹及其周围的总体炎症和浆细胞数量显著增加。此外,尽管AIP、IDC和CP之间壶腹和十二指肠组织中IgG4+浆细胞的原始数量存在一些重叠,但IgG4/IgG比例,尤其是壶腹的该比例,在鉴别AIP与其他“肿块形成”病变方面似乎具有诊断价值。当应用0.10的临界值时,壶腹IgG4/IgG比例的诊断敏感性和特异性分别为86%和95%。总之,评估壶腹组织学和IgG4/IgG比例可能有助于鉴别AIP与其他胰腺肿块形成病变。