自身免疫性胰腺炎
医学
胰腺炎
胰腺癌
疾病
IgG4相关疾病
胰腺
炎症性肠病
血清学
病理
胃肠病学
内科学
免疫学
癌症
抗体
作者
Nicolò de Pretis,Antonio Amodio,Giulia De Marchi,Eugenio Marconato,Rachele Ciccocioppo,Luca Frulloni
标识
DOI:10.1080/1744666x.2022.2125379
摘要
Introduction Autoimmune pancreatitis (AIP) is a fibroinflammatory disease of the pancreas. Type 1 AIP is the pancreatic manifestation of a systemic IgG4-related disease and is associated with serum elevation of IgG4, tissue infiltration of IgG4-positive plasma cells, and multiorgan involvement. Although serum IgG4 elevation is considered a useful diagnostic tool, the concomitant presence of more diagnostic criteria is needed to achieve diagnosis. No other biomarkers have been approved in clinical practice in type 1 AIP. Type 2 AIP is a pancreatic-specific disease associated with inflammatory bowel disease. No specific biomarkers for type 2 AIP have been identified.Areas covered The role of serum IgG4 in the diagnosis, management and follow-up of patients with type 1 AIP. Moreover, data on other emerging biomarkers for type 1 and 2 AIP have been reported.Expert Opinion The diagnosis of AIP is challenging in clinical practice, especially for focal forms without multiorgan involvement, where distinction from pancreatic cancer can be difficult. Despite the strong association with type 1 AIP, serum IgG4 should only be measured when the suspicion for the disease is high, considering its limited sensitivity. New biomarkers with high diagnostic yield for both type 1 and type 2 AIP are needed.
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