Irie Hiroyuki, Yoshimitsu Kengo, Aibe Hitoshi, Tajima Tsuyoshi, Nishie Akihiro, Nakayama Tomohiro, Kakihara Daisuke, Honda Hiroshi
Department of Clinical Radiology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
J Comput Assist Tomogr. 2004 Jan-Feb;28(1):117-22. doi: 10.1097/00004728-200401000-00020.
The purpose of this study was to elucidate the natural history of branch duct type pancreatic intraductal papillary mucinous tumor (IPMT) by evaluating serial changes in the magnetic resonance cholangiopancreatography (MRCP) findings of patients diagnosed with pancreatic IPMT of branch duct type.
Thirty-five patients had branch duct type IPMT, including 9 patients with separate lesions, and underwent initial and follow-up MRCP over a period of more than 12 months. The maximum diameter of the cystic lesion, the presence of associated main pancreatic duct (MPD) dilatation, and the presence of a filling defect were evaluated. Serial changes in these findings were analyzed.
Tumor enlargement on follow-up MRCP was observed in 7 cases. Of the 29 branch duct IPMTs without associated MPD dilatation or a filling defect identified on initial MRCP, only 1 showed gradual tumor enlargement. In 4 cases, the cyst size decreased on follow-up MRCP.
Branch duct type IPMTs grow slowly and can be monitored without operation provided that the tumor shows no associated MPD dilatation or filling defect.
本研究的目的是通过评估经诊断为分支导管型胰腺导管内乳头状黏液性肿瘤(IPMT)患者的磁共振胰胆管造影(MRCP)结果的系列变化,以阐明分支导管型IPMT的自然病程。
35例患者患有分支导管型IPMT,其中9例为孤立性病变,在超过12个月的时间里接受了初次和随访MRCP检查。评估了囊性病变的最大直径、是否存在相关主胰管(MPD)扩张以及是否存在充盈缺损。分析了这些结果的系列变化。
7例患者在随访MRCP中观察到肿瘤增大。在初次MRCP中未发现相关MPD扩张或充盈缺损的29例分支导管型IPMT中,只有1例显示肿瘤逐渐增大。4例患者在随访MRCP中囊肿大小减小。
分支导管型IPMT生长缓慢,只要肿瘤未显示相关MPD扩张或充盈缺损,就可以在不进行手术的情况下进行监测。