H. Irie et al., MR cholangiopancreatographic differentiation of benign and malignant intraductal mucin-producing tumors of the pancreas, AM J ROENTG, 174(5), 2000, pp. 1403-1408
Citations number
30
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
OBJECTIVE, The purpose of this study was to establish MR cholangiopancreato
graphic criteria for discriminating benign from malignant intraductal mucin
-producing tumors of the pancreas.
MATERIALS AND METHODS, Thirty-one patients with 34 intraductal mucin-produc
ing tumors underwent MR cholangiopancreatography. Tumors were classified as
either main duct type (n = 10) or branch duct type (n = 24). In patients w
ith the main duct type, the maximum diameter and the location of the main p
ancreatic duct, the extent of main pancreatic duct dilatation, and the pres
ence of a filling defect were evaluated. For branch duct type, the location
and maximum diameter of the cystic lesion, the presence of a filling defec
t, and the presence of associated main pancreatic duct dilatation were eval
uated.
RESULTS. In patients with the main duct type, the main pancreatic duct was
significantly narrower when associated with benign rather than malignant tu
mors. All malignant tumors showed diffuse main pancreatic duct dilatation,
whereas arl benign tumors showed segmental dilatation. Among patients with
branch duct type, the cyst was smaller when it was a benign rather than mal
ignant tumor. All but one malignant tumor showed mild associated main pancr
eatic duct dilatation, whereas benign tumors were not associated with main
pancreatic duct dilatation. Filling defects suggested malignancy, although
half of the malignant tumors had no filling defects.
CONCLUSION. In patients with intraductal mucin-producing tumors of the panc
reas, tilling defects are indicative of malignancy. Diffuse main pancreatic
duct dilatation greater than 15 mm (main duct type), or any main pancreati
c duct dilatation (branch duct type), is strongly associated with malignanc
y.