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IgG4阳性浆细胞浸润在自身免疫性胰腺炎诊断中的作用

IgG4-positive plasma cell infiltration in the diagnosis of autoimmune pancreatitis.

作者信息

Zhang Lizhi, Notohara Kenji, Levy Michael J, Chari Suresh T, Smyrk Thomas C

机构信息

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Mod Pathol. 2007 Jan;20(1):23-8. doi: 10.1038/modpathol.3800689. Epub 2006 Sep 15.

Abstract

Autoimmune pancreatitis typically produces an enlarged pancreas with narrowing of the pancreatic duct, and can mimic carcinoma. Autoimmune pancreatitis usually responds to corticosteroid treatment, making it important to differentiate from pancreatic ductal adenocarcinoma. Affected patients often have an elevated serum IgG4. It has been proposed that increased numbers of IgG4-positive plasma cells in tissue might be a marker for the condition. We investigated the role of IgG4 staining in the diagnosis of autoimmune pancreatitis, first in resected pancreas specimens (29 autoimmune pancreatitis, nine chronic alcoholic pancreatitis and 25 pancreatic cancer), then in pancreatic needle biopsies. Immunohistochemical stains for IgG4 were scored as none, mild, moderate or marked, according to published criteria. Moderate to marked numbers of IgG4-positive plasma cells were seen in 21/29 autoimmune pancreatitis patients, and were distributed in and around ducts, in interlobular fibrous tissue and in peripancreatic fat. In contrast, eight of nine examples of chronic alcoholic pancreatitis and 22/25 ductal adenocarcinomas had scores of none or mild. When we subdivided autoimmune pancreatitis into the histologic subtypes lymphoplasmacytic sclerosing pancreatitis and idiopathic duct-destructive pancreatitis, 16/17 lymphoplasmacytic sclerosing pancreatitis had moderate to marked staining, compared to five to 12 idiopathic duct-destructive pancreatitis. Needle biopsies from nine patients suspected of having autoimmune pancreatitis had increased numbers of IgG4 cells. We conclude that pancreatic tissue from patients with autoimmune pancreatitis often shows moderate or marked infiltration by IgG4-positive plasma cells (>10/HPF). This is particularly so in the subtype we have designated lymphoplasmacytic sclerosing pancreatitis. We rarely see IgG4 staining in patients with chronic alcoholic pancreatitis and pancreatic ductal adenocarcinoma. IgG4-positive plasma cells are a useful marker for the tissue diagnosis of autoimmune pancreatitis.

摘要

自身免疫性胰腺炎通常会导致胰腺肿大并伴有胰管狭窄,且可能类似癌症。自身免疫性胰腺炎通常对皮质类固醇治疗有反应,因此将其与胰腺导管腺癌区分开来很重要。受影响的患者血清IgG4通常会升高。有人提出组织中IgG4阳性浆细胞数量增加可能是该病的一个标志物。我们首先在切除的胰腺标本(29例自身免疫性胰腺炎、9例慢性酒精性胰腺炎和25例胰腺癌)中研究了IgG4染色在自身免疫性胰腺炎诊断中的作用,然后在胰腺穿刺活检中进行了研究。根据已发表的标准,IgG4的免疫组织化学染色分为无、轻度、中度或重度。21/29例自身免疫性胰腺炎患者可见中度至重度数量的IgG4阳性浆细胞,分布于导管内及周围、小叶间纤维组织和胰腺周围脂肪中。相比之下,9例慢性酒精性胰腺炎中有8例以及25例导管腺癌中有22例的染色评分为无或轻度。当我们将自身免疫性胰腺炎细分为组织学亚型淋巴浆细胞性硬化性胰腺炎和特发性导管破坏性胰腺炎时,16/17例淋巴浆细胞性硬化性胰腺炎有中度至重度染色,而特发性导管破坏性胰腺炎为5至12例。9例疑似自身免疫性胰腺炎患者的穿刺活检中IgG4细胞数量增加。我们得出结论,自身免疫性胰腺炎患者的胰腺组织通常显示IgG4阳性浆细胞的中度或重度浸润(>10/HPF)。在我们指定的淋巴浆细胞性硬化性胰腺炎亚型中尤其如此。我们在慢性酒精性胰腺炎和胰腺导管腺癌患者中很少见到IgG4染色。IgG4阳性浆细胞是自身免疫性胰腺炎组织诊断的有用标志物。

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