Gourgiotis S, Ridolfini M P, Germanos S
Hepatobiliary and Pancreatic Surgery Department, Royal London Hospital, Whitechapel, London E1 1BB, UK.
Eur J Surg Oncol. 2007 Aug;33(6):678-84. doi: 10.1016/j.ejso.2006.11.031. Epub 2007 Jan 4.
BACKGROUND/AIMS: Intraductal papillary mucinous neoplasms (IPMNs) are neoplasms of the pancreatic duct epithelium characterized by intraductal papillary growth and thick mucin secretion. Quantities of mucin fill the main and/or branches of pancreatic ducts and cause ductal dilatation. This review encompasses IPMNs, including symptoms, diagnosis, management, and prognosis.
A Pubmed database search was performed. All abstracts were reviewed and all articles in which cases of IPMNs could be identified were further scrutinized. Further references were extracted by cross-referencing.
Only one-third of all patients are symptomatic. According to the site of involvement, IPMNs are classified into three types: main duct type, branch duct type, and combined type. Most branch type IPMNs are benign, while the other two types are frequently malignant. The presence of large mural nodules increases the possibility of malignancy in all types. Presence of a large branch type IPMN and marked dilatation of the main duct indicate the existence of adenoma at least. Synchronous or metachronous malignancies may be developed in various organs. Endoscopic retrograde cholangiopancreatography, endoscopic ultrasonography, and intraductal ultrasonography clearly demonstrate ductal dilatation and mural nodules, while magnetic resonance pancreatography best visualizes the entire outline of IPMNs.
Prognosis is excellent after complete resection of benign and non-invasive malignant IPMNs. The extent of pancreatic resection and the intraoperative management of resection margins remain controversial. Total pancreatectomy should be reserved for patients with resectable but extensive IPMNs involving the whole pancreas; its benefits, however, must be balanced against operative and postoperative risks. Regular monitoring for disease recurrence is important after surgery.
背景/目的:导管内乳头状黏液性肿瘤(IPMNs)是胰腺导管上皮的肿瘤,其特征为导管内乳头状生长和大量黏液分泌。大量黏液充满胰腺导管的主支和/或分支,导致导管扩张。本综述涵盖IPMNs,包括症状、诊断、治疗和预后。
进行了PubMed数据库检索。对所有摘要进行了审查,并对所有能识别出IPMNs病例的文章进行了进一步仔细研究。通过交叉引用提取了更多参考文献。
所有患者中只有三分之一有症状。根据受累部位,IPMNs分为三种类型:主胰管型、分支胰管型和混合型。大多数分支型IPMNs是良性的,而其他两种类型通常是恶性的。大的壁内结节的存在增加了所有类型中发生恶性肿瘤的可能性。存在大的分支型IPMN和主胰管明显扩张至少表明存在腺瘤。可能在各个器官发生同步或异时性恶性肿瘤。内镜逆行胰胆管造影、内镜超声和管内超声能清楚显示导管扩张和壁内结节,而磁共振胰胆管造影能最佳显示IPMNs的整体轮廓。
良性和非侵袭性恶性IPMNs完整切除后的预后良好。胰腺切除的范围和切除边缘的术中处理仍存在争议。全胰切除术应仅用于可切除但广泛累及全胰腺的IPMNs患者;然而,其益处必须与手术和术后风险相权衡。术后定期监测疾病复发很重要。