4.3 Article

Clinical differences between mass-forming autoimmune pancreatitis and pancreatic cancer

期刊

SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
卷 47, 期 5, 页码 607-613

出版社

TAYLOR & FRANCIS LTD
DOI: 10.3109/00365521.2012.667147

关键词

autoimmune pancreatitis; diagnostic criteria; mass-forming; pancreatic cancer

资金

  1. Ministry of Culture and Science of Japan [23790803, 23591015]
  2. Ministry of Health, Labor, and Welfare of Japan
  3. Grants-in-Aid for Scientific Research [23790803, 23591015] Funding Source: KAKEN

向作者/读者索取更多资源

Objective. Autoimmune pancreatitis (AIP) needs to be differentiated from pancreatic cancer (PC). We aimed to clarify the findings specific for AIP by comparing the clinical differences between mass-forming AIP and PC. Material and methods. We retrospectively compared 36 patients with mass-forming AIP and 60 with PC without metastasis regarding clinical, imaging, serological, histological differences and other organ involvement (OOI). We evaluated the sensitivity, specificity and accuracy of these findings for the differential diagnosis between AIP and PC. Results. The findings 100% specific for AIP were a capsule-like rim on computed tomography (CT), skipped lesion of main pancreatic duct (MPD) on endoscopic retrograde pancreatography (ERP) or magnetic resonance cholangiopancreatography (MRCP), gamma-globulin > 2 g/dl, OOI (extrapancreatic biliary stricture, salivary gland swelling and retroperitoneal fibrosis) and ruling out PC by histopathological findings of endoscopic ultrasonography-guided fine-needle aspiration. The findings over 90% specific were IgG4 > 280 mg/dl (98%), IgG > 1800 mg/dl (97%), maximal diameter of upstream MPD < 5 mm on MRCP (95%) and IgG4 > 135 mg/dl (94%), respectively. Conclusions. Clinical, imaging, serological, histological findings and OOI differed between mass-forming AIP and PC. Capsule-like rim on CT, skipped lesion of MPD on ERP or MRCP, IgG4 > 280 mg/dl, and OOI were highly specific findings for AIP. These findings are useful in the differential diagnosis of mass-forming AIP from PC.

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