|
Intraductal papillary mucinous tumor (IPMT) of the pancreas is
a mucin-producing tumor which arises from the epithelial lining
of the pancreatic ducts. The dysplastic epithelium proliferates
and forms papillary projections that protrude into and expand the
main pancreatic ducts and/or side branch ducts. Duct obstruction
is secondary to plugs of mucin elaborated by the epithelium or ductal
compression by cystic masses.
The average age at diagnosis is 65 years (range 30-94 years) with
a female predominance. The etiology and risk factors are unknown.
IPMT can be benign or malignant according to its pathological features,
including benign hyperplasia adenoma, borderline low grade dysplasia
adenoma, high grade dysplasia adenoma (carcinoma in situ), and malignant
adenocarcinoma. Differential diagnosis of IPMT of the pancreas includes
chronic pancreatitis, mucinous cystadenoma, cystadenocarcinoma,
serous cystadenoma, and pancreatic pseudocyst. Clinical symptoms
and signs of IPMT include pancreatitis-like abdominal pain, diarrhea/steatorrhea,
and obstructive jaundice, which are caused by thick mucinous ductual
obstruction, and diabetes mellitus. Predictive signs of malignancy
of IPMT are presence of diabetes mellitus, male gender, marked and
diffuse dilatation of main pancreatic duct (>10mm), presence
of large mural nodules (> 10 mm), and tumor arising from the
head of the pancreas.
IPMTs may be classified into main duct, branch duct, or combined
types. Main pancreatic duct type involvement presents as diffuse
or segmental ductal dilatation, copious mucin production, papillary
growth, and is typically associated with malignancy. These tumors
exhibit a greatly expanded main pancreatic duct ranging from 3-10
cm and this severe ductal dilatation is easily mistaken as cystic
neoplasm. Branch duct type IPMT predominantly involves the side
branch ducts and appear as oval-shaped cystic masses in proximity
to the main pancreatic duct. These benign tumors appear as localized
cystic parenchymal lesions. The majority of branch duct type IPMTs
are located in the uncinate process of the pancreas. The combined
type IPMT involves both the main and branch ducts, as in this case.
The following findings are seen on imaging studies: lobulated
multicystic dilatation of the branch ducts, diffuse dilatation of
the main pancreatic duct, intraductal papillary tumors, elongated
or glob-like mucous plugs in the dilated ducts, and bulging of the
papilla into the duodenal lumen. The diagnosis of IPMT can be suggested
using ultrasonography, CT, or magnetic resonance colangiopancreatography
(MRCP). Endoscopic retrograde cholangiopancreatography (ERCP) has
traditionally been the imaging modality of choice for diagnosis
because it depicts the communication between the cystically dilated
main pancreatic ducts, as well as, intraductal papillary tumor and
mucous plugs. MRCP provides a non-invasive method for tumor imaging.
MRCP can be preformed using half-Fourier single shot fast spin echo
technique (HASTE) with a high sensitivity to detect main pancreatic
duct and its branch dilatations.
References:
- Semelka RC. Abdominal-Pelvic MRI. New York: Wiley-Liss Inc,
c2002. pp. 444-445.
- Lim JH, Lee G, and Oh YL. Radiologic Spectrum of Intraductal
Papillary Mucinous Tumor of the Pancreas. Radiographics.
2001; 21: 323-340.
- Chan W, Wong T, and Tzeng B. Intraductal Papillary Mucinous
Tumors of the Pancreas: A Case Report. Chinese Journal of
Radiology. 2002; 27: 311-314.
|