Affiliations 

  • 1 Medical Department 2, Caritas-Krankenhaus, Bad Mergentheim, Germany
  • 2 Department of Internal Medicine, Krankenhaus Märkisch Oderland, Strausberg/Wriezen, Germany
  • 3 Pancreato-Biliary Endoscopy and Endosonography Division, Vita Salute San Raffaele University, Milan, Italy
  • 4 Department of Internal Medicine 2, Helios Hospital Meiningen GmbH, Meiningen, Germany
  • 5 Medical Department I/Gastroenterology, SANA Hospital Lichtenberg, Berlin, Germany
  • 6 Department of Gastroenterology, Research Center of Gastroenterology and Hepatology, University of Medicine and Pharmacy, Craiova, Romania
  • 7 SRH Wald Klinikum Gera, Germany
  • 8 Gastroenterology Unit, Department of Medical and Surgical Sciences University of Bologna, Hospital of Imola, Italy
  • 9 Gastroenterology and Hepatology Department, University Hospital, Santiago de Compostela, Spain
  • 10 Division of Gastroenterology, Prince Court Medical Centre, Kuala Lumpur, Malaysia
  • 11 Translational Gastroenterology Unit, Oxford University Hospitals NHS Foundation Trust, Oxford, UK
  • 12 Medical Department I, Sana Hospital Lübeck, Germany
  • 13 Department of Ultrasound, Zhongshan Hospital, Fudan University, Shanghai, China
Endoscopy, 2018 11;50(11):1071-1079.
PMID: 29689572 DOI: 10.1055/a-0588-4941

Abstract

BACKGROUND: The prevalence of malignancy in patients with small solid pancreatic lesions is low; however, early diagnosis is crucial for successful treatment of these cases. Therefore, a method to reliably distinguish between benign and malignant small solid pancreatic lesions would be highly desirable. We investigated the role of endoscopic ultrasound (EUS) elastography in this setting.

METHODS: Patients with solid pancreatic lesions ≤ 15 mm in size and a definite diagnosis were included. Lesion stiffness relative to the surrounding pancreatic parenchyma, as qualitatively assessed and documented at the time of EUS elastography, was retrospectively compared with the final diagnosis obtained by fine-needle aspiration/biopsy or surgical resection.

RESULTS: 218 patients were analyzed. The average size of the lesions was 11 ± 3 mm; 23 % were ductal adenocarcinoma, 52 % neuroendocrine tumors, 8 % metastases, and 17 % other entities; 66 % of the lesions were benign. On elastography, 50 % of lesions were stiffer than the surrounding pancreatic parenchyma (stiff lesions) and 50 % were less stiff or of similar stiffness (soft lesions). High stiffness of the lesion had a sensitivity of 84 % (95 % confidence interval 73 % - 91 %), specificity of 67 % (58 % - 74 %), positive predictive value (PPV) of 56 % (50 % - 62 %), and negative predictive value (NPV) of 89 % (83 % - 93 %) for the diagnosis of malignancy. For the diagnosis of pancreatic ductal adenocarcinoma, the sensitivity, specificity, PPV, and NPV were 96 % (87 % - 100 %), 64 % (56 % - 71 %), 45 % (40 % - 50 %), and 98 % (93 % - 100 %), respectively.

CONCLUSIONS: In patients with small solid pancreatic lesions, EUS elastography can rule out malignancy with a high level of certainty if the lesion appears soft. A stiff lesion can be either benign or malignant.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.