Search tips
Search criteria 


Logo of worldjgastrosurgLink to Publisher's site
World J Gastrointest Surg. 2010 October 27; 2(10): 342–346.
Published online 2010 October 27. doi:  10.4240/wjgs.v2.i10.342
PMCID: PMC2999210

Differences between main-duct and branch-duct intraductal papillary mucinous neoplasms of the pancreas


In the last decade, intraductal papillary mucinous neoplasms (IPMNs) have become commonly diagnosed. From a morphological standpoint, they are classified in main-duct IPMNs (MD-IPMNs) and branch-duct IPMNs (BD-IPMNs), depending on the type of involvement of the pancreatic ductal system by the neoplasm. Despite the fact that our understanding of their natural history is still incomplete, recent data indicate that MD-IPMNs and BD-IPMNs show significant differences in terms of biological behaviour with MD-IPMNs at higher risk of malignant degeneration. In the present paper, clinical and epidemiological characteristics, rates of malignancy and the natural history of MD-IPMNs and BD-IPMNs are analyzed. The profile of IPMNs involving both the main pancreatic duct and its side branches (combined-IPMNs) are also discussed. Finally, general recommendations for management based on these differences are given.

Keywords: Intraductal papillary mucinous neoplasms, Branch-duct, Main-duct, Malignancy, Surgery, Follow-up, Nodules, Combined type


In 1982, Ohhashi et al[1] from Japan described four cases of pancreatic cancer characterized by overproduction of mucus, diffuse dilatation of the pancreatic ductal system and presence of bulging papilla. In the next decade, small case reports from Europe and the United States referred to this condition as “mucinous ductal ectasia”[2-4]. Only in 1996 were these lesions defined as intraductal papillary mucinous neoplasms (IPMNs) by the World Health Organization (WHO) classification for tumors of the exocrine pancreas[5]. Main-duct IPMNs (MD-IPMNs) are characterized by involvement of the main pancreatic duct with or without associated involvement of the branch ducts (combined IPMNs); they usually present as a dilated (≥ 1 cm) main pancreatic duct or as cystic dilation of the main duct and its branches; branch-duct IPMNs (BD-IPMNs) originate in the side branches of the pancreatic ductal system, appearing as a cystic lesion that always communicates with a non-dilated main pancreatic duct[6].

In the last ten years, the diagnosis of IPMNs has significantly increased[7,8]. This can be related to improved imaging techniques, greater awareness of this condition by the gastroenterological community and incidental diagnosis among asymptomatic individuals.

The distinction among different IPMN sub-types is not only of “morphological” significance but has a practical impact on the management of patients with IPMNs. In this paper, we will review the clinico-pathological and epidemiological characteristics of IPMNs, their natural history and risk of malignancy with some guidelines for their management.


IPMNs are typically found in elderly people. In most series, the median age of patients at the diagnosis is 65-70 years[6,8-19]. However, while a few studies made a clear distinction between MD-IPMNs and BD-IPMNs, most series include both subgroups. We recently have analyzed the clinical and epidemiological characteristics of a large series of IPMNs who underwent surgical resection at the University of Verona and at the Massachusetts General Hospital[20]. One hundred and fifty-nine patients had histologically confirmed BD-IPMNs while 81 had MD-IPMNs. Median age at presentation was similar in the two groups (66 and 67 years respectively) as well as a family history of pancreatic cancer (7.5% of MD-IPMNs and 11% of BD-IPMNs) and the presence of extra-pancreatic neoplasms (22% of MD-IPMNs and 20% of BD-IPMNs). The most common extra-pancreatic neoplasms were breast, colorectal, lung and prostate cancer. Other reports suggest that patients with IPMNs are at higher risk of developing extra-pancreatic tumors if compared with the general population and, in keeping with our data, colorectal cancer and adenomatous polyps are commonly found in IPMNs patients[21-24]. Interestingly, BD-IPMNs were most commonly found in females (57%) and MD-IPMNs in males (55.5%). BD-IPMNs and MD-IPMNs were found in the proximal pancreas in 64% and 52% of cases respectively and BD-IPMNs were more frequently associated with a diffuse pattern (23% vs 4%)[20].

Moreover, while BD-IPMNs are characterized by the presence of multifocal cystic lesions in different sites of the gland (sometimes with a complete involvement of the entire pancreas), MD-IPMNs spread along the main pancreatic duct, also possibly being skip lesions[25].

Clinically, BD-IPMNs were more frequently discovered in asymptomatic individuals (34.5% vs 13.5%). Abdominal pain was common in both MD-IPMNs and BD-IPMNs but in many cases it was an aspecific symptom. On the other hand, more specific and objective symptoms such as jaundice and weight loss were significantly associated with the presence of MD-IPMNs[20]. The main features of both IPMNs are briefly summarized in Table Table11.

Table 1
Epidemiological and clinicopathological characteristics of patients with main-duct, branch-duct and combined intraductal papillary mucinous neoplasms n,%


Our knowledge of the natural history of IPMNs is still incomplete but a better awareness of the distinction between the main and branch duct variants have contributed to a better understanding. It is well known that IPMNs can show a series of dysplastic changes from adenoma to invasive carcinoma and that different degrees of dysplasia can be found within the same lesion[5,6,26,27]. The frequency of malignancy (in-situ and invasive carcinoma) in MD-IPMNs is high, ranging between 60% and 92% with a mean of 70%[6,10,16-19]. The largest published series on MD-IPMNs combines the experience of Massachusetts General Hospital and University of Verona with 140 resected patients[18]. In this study, we found that patients with malignant MD-IPMNs were significantly older by 6.4 years than those with benign ones. The experiences from Johns Hopkins[10] and Indiana University[16] confirmed this observation, showing that patients with MD-IPMNs with invasive cancer are older than those with noninvasive neoplasms by 5 years. These findings suggest that most, if not all, MD-IPMNs can progress to malignancy.

By contrast, in BD-IPMNs the frequency of malignancy is significantly lower (between 6% and 46%, with a mean of 25%) and that of invasive cancer ranges from 0 to 30% (mean of 15%)[6,8,9,10-16]. In the combined experience of Massachusetts General Hospital and University of Verona, 145 patients underwent surgical resection for BD-IPMNs[9]. Of these, 32 (22%) had malignancy but there was invasive carcinoma in only 11% (16 patients) with no age difference between benign and malignant tumors (66 years vs 67.5 years). Schmidt et al[16] and Peleaz-Luna et al[13] reported a rate of malignancy of only 19% and 12% in their series of 103 and 77 patients who underwent surgery for BD-IPMNs. Levy et al[12] calculated the longitudinal risk of malignant transformation since the first clinical or radiological sign in a series of 106 patients with histologically proven IPMNs or probable IPMN (30 patients with a radiological diagnosis of BD-IPMNs). Overall ten year actuarial risk of occurrence of IPMNs with low-grade dysplasia, high-grade dysplasia and invasive cancer was 67%, 49% and 29% respectively. Five year actuarial risk of malignancy was 15% for BD-IPMNs and 63% for MD-IPMNs (P < 0.001).


Combined-IPMNs are characterized by an involvement of both the main pancreatic duct and the branch-ducts of the pancreas by the tumor. Combined-IPMNs have historically been considered as an extension of MD-IPMNs into the side branches of the ductal system[6,18]. However, it is unclear if combined-IPMNs represent a progression of MD-IPMNs, a progression of multifocal BD-IPMNs or if they represent a disease itself with a specific profile. In this light, we have recently compared the clinical and epidemiological characteristics of 159 patients with BD-IPMNs, 81 MD-IPMNs and 149 combined-IPMNs in order to elucidate differences among the three groups[20]. All these patients underwent surgical resection and therefore a histological diagnosis was available. Interestingly, combined-IPMNs showed close overlapping similarities with MD-IPMNs with regard to clinico-pathological and epidemiological characteristics. For example we found that MD-IPMNs and combined-IPMNs have the same sex ratio (female 44%, male 54%) opposite to that of BD-IPMNs. While the median age at presentation was similar in the three groups, patients with MD-IPMNs and combined-IPMNs with invasive cancer were significantly older than those with noninvasive neoplasms, suggesting tumor progression. As previously described, BD-IPMNs were more likely asymptomatic whereas the majority of patients with MD-IPMNs and combined-IPMNs were symptomatic. Finally, most patients with BD-IPMNs had an adenoma (44%) with a low prevalence of cancer (overall malignancy 22%, invasive cancer 11%). On the other hand, MD-IPMNs and combined-IPMNs contained malignant elements in 68% and 62% respectively, with invasive cancer present in 48% and 42%. Considering all these findings, we conclude that combined-IPMNs can be considered a sub-group of MD-IPMNs. The presence of an age difference between non-invasive and invasive tumors and the high frequency of malignancy in MD-IPMNs and combined-IPMNs[10,18,20] suggest that these IPMNs subtypes share an aggressive biology characterized by progression to invasive cancer.


Based on morphological criteria and mucin expression, IPMNs can be classified in four subtypes including gastric, intestinal, pancreatobiliary and oncocytic types[6,27]. Ban et al[28] evaluated the features of 80 gastric-type IPMNs and of 30 with intestinal-type. They showed that gastric-type IPMNs were mostly BD-IPMNs (98%) and were associated with high-grade dysplasia or invasive cancer in only 8% of cases whereas the intestinal-type IPMNs were usually MD-IPMNs (73%) and had malignancy in 80% of cases. They also showed that intestinal-type IPMNs were characterized by MUC2 expression and that low-grade PanIN complexes were typical features of gastric-type IPMNs. These authors concluded that gastric and intestinal-type IPMNs have distinct histopathological features and mucin profiles, perhaps suggesting that they follow different biological pathways. This in turn may account for the clinical differences between BD-IPMNs and MD-IPMNs.

Unfortunately, specific genetic analysis in order to elucidate differences in the biological behavior among MD-IPMNs, BD-IPMNs and combined-IPMNs has not been published yet.


Briefly, the differences in clinical-pathological characteristics, risk of malignancy and biological behavior between MD-IPMNs (including the combined-type) and BD-IPMNs have a strong impact on their clinical management. Considering the high prevalence of malignancy/invasive carcinoma in MD-IPMNs and the lack of clinical and radiological parameters predictive of malignancy, all of these lesions in surgically fit patients have to be resected[6,10,16-19]. On the other hand, several studies demonstrated that BD-IPMNs less than 3 cm in size, without nodules and with no symptoms can be carefully managed in a surveillance program whereas surgical resection is indicated for any symptomatic lesion, for BD-IPMNs with a median diameter more than 3 cm and in the presence of nodules because these parameters are more frequently associated with a potential risk of malignancy[6,8,9,10-15].


Peer reviewer: Shailesh V Shrikhande, MS, MD, Professor, Department of Gastrointestinal and Hepato-Pancreato-Biliary Surgery, Tata Memorial Hospital Ernest Borges Marg, Parel, Mumbai 400012, India

S- Editor Wang JL L- Editor Roemmele A E- Editor Yang C


1. Ohhashi K, Murakami Y, Maruyama M, Takekoshi T, Ohta H, Ohhashi I, Takagi K, Kato Y. Four cases of mucous secreting pancreatic cancer. Prog Dig Endosc. 1982;20:348–351.
2. Warshaw AL, Compton CC, Lewandrowski K, Cardenosa G, Mueller PR. Cystic tumors of the pancreas. New clinical, radiologic, and pathologic observations in 67 patients. Ann Surg. 1990;212:432–443; discussion 444-445. [PubMed]
3. Yamaguchi K, Tanaka M. Mucin-hypersecreting tumor of the pancreas with mucin extrusion through an enlarged papilla. Am J Gastroenterol. 1991;86:835–839. [PubMed]
4. Kawarada Y, Yano T, Yamamoto T, Yokoi H, Imai T, Ogura Y, Mizumoto R. Intraductal mucin-producing tumors of the pancreas. Am J Gastroenterol. 1992;87:634–638. [PubMed]
5. Kloppel G, Solcia , E , Longnecker DS, Capella C, Sobin LH. World Health Organization International Histological Typing of Tumors of the Exocrine Pancreas. Berlin: Springer–Verlag; 1996. pp. 1–61.
6. Tanaka M, Chari S, Adsay V, Fernandez-del Castillo C, Falconi M, Shimizu M, Yamaguchi K, Yamao K, Matsuno S. International consensus guidelines for management of intraductal papillary mucinous neoplasms and mucinous cystic neoplasms of the pancreas. Pancreatology. 2006;6:17–32. [PubMed]
7. Fernández-del Castillo C, Targarona J, Thayer SP, Rattner DW, Brugge WR, Warshaw AL. Incidental pancreatic cysts: clinicopathologic characteristics and comparison with symptomatic patients. Arch Surg. 2003;138:427–433; discussion 433-434. [PubMed]
8. Salvia R, Crippa S, Falconi M, Bassi C, Guarise A, Scarpa A, Pederzoli P. Branch-duct intraductal papillary mucinous neoplasms of the pancreas: to operate or not to operate? Gut. 2007;56:1086–1090. [PMC free article] [PubMed]
9. Rodriguez JR, Salvia R, Crippa S, Warshaw AL, Bassi C, Falconi M, Thayer SP, Lauwers GY, Capelli P, Mino-Kenudson M, et al. Branch-duct intraductal papillary mucinous neoplasms: observations in 145 patients who underwent resection. Gastroenterology. 2007;133:72–79; quiz 309-310. [PubMed]
10. Sohn TA, Yeo CJ, Cameron JL, Hruban RH, Fukushima N, Campbell KA, Lillemoe KD. Intraductal papillary mucinous neoplasms of the pancreas: an updated experience. Ann Surg. 2004;239:788–797; discussion 797-799. [PubMed]
11. Tanno S, Nakano Y, Nishikawa T, Nakamura K, Sasajima J, Minoguchi M, Mizukami Y, Yanagawa N, Fujii T, Obara T, et al. Natural history of branch duct intraductal papillary-mucinous neoplasms of the pancreas without mural nodules: long-term follow-up results. Gut. 2008;57:339–343. [PubMed]
12. Lévy P, Jouannaud V, O'Toole D, Couvelard A, Vullierme MP, Palazzo L, Aubert A, Ponsot P, Sauvanet A, Maire F, et al. Natural history of intraductal papillary mucinous tumors of the pancreas: actuarial risk of malignancy. Clin Gastroenterol Hepatol. 2006;4:460–468. [PubMed]
13. Pelaez-Luna M, Chari ST, Smyrk TC, Takahashi N, Clain JE, Levy MJ, Pearson RK, Petersen BT, Topazian MD, Vege SS, et al. Do consensus indications for resection in branch duct intraductal papillary mucinous neoplasm predict malignancy? A study of 147 patients. Am J Gastroenterol. 2007;102:1759–1764. [PubMed]
14. Rautou PE, Lévy P, Vullierme MP, O'Toole D, Couvelard A, Cazals-Hatem D, Palazzo L, Aubert A, Sauvanet A, Hammel P, et al. Morphologic changes in branch duct intraductal papillary mucinous neoplasms of the pancreas: a midterm follow-up study. Clin Gastroenterol Hepatol. 2008;6:807–814. [PubMed]
15. Tang RS, Weinberg B, Dawson DW, Reber H, Hines OJ, Tomlinson JS, Chaudhari V, Raman S, Farrell JJ. Evaluation of the guidelines for management of pancreatic branch-duct intraductal papillary mucinous neoplasm. Clin Gastroenterol Hepatol. 2008;6:815–819; quiz 719. [PubMed]
16. Schmidt CM, White PB, Waters JA, Yiannoutsos CT, Cummings OW, Baker M, Howard TJ, Zyromski NJ, Nakeeb A, DeWitt JM, et al. Intraductal papillary mucinous neoplasms: predictors of malignant and invasive pathology. Ann Surg. 2007;246:644–651; discussion 651-654. [PubMed]
17. Schnelldorfer T, Sarr MG, Nagorney DM, Zhang L, Smyrk TC, Qin R, Chari ST, Farnell MB. Experience with 208 resections for intraductal papillary mucinous neoplasm of the pancreas. Arch Surg. 2008;143:639–646; discussion 646. [PubMed]
18. Salvia R, Fernández-del Castillo C, Bassi C, Thayer SP, Falconi M, Mantovani W, Pederzoli P, Warshaw AL. Main-duct intraductal papillary mucinous neoplasms of the pancreas: clinical predictors of malignancy and long-term survival following resection. Ann Surg. 2004;239:678–685; discussion 685-687. [PubMed]
19. D'Angelica M, Brennan MF, Suriawinata AA, Klimstra D, Conlon KC. Intraductal papillary mucinous neoplasms of the pancreas: an analysis of clinicopathologic features and outcome. Ann Surg. 2004;239:400–408. [PubMed]
20. Crippa S, Fernández-Del Castillo C, Salvia R, Finkelstein D, Bassi C, Domínguez I, Muzikansky A, Thayer SP, Falconi M, Mino-Kenudson M, et al. Mucin-producing neoplasms of the pancreas: an analysis of distinguishing clinical and epidemiologic characteristics. Clin Gastroenterol Hepatol. 2010;8:213–219. [PubMed]
21. Reid-Lombardo KM, Mathis KL, Wood CM, Harmsen WS, Sarr MG. Frequency of extrapancreatic neoplasms in intraductal papillary mucinous neoplasm of the pancreas: implications for management. Ann Surg. 2010;251:64–69. [PubMed]
22. Baumgaertner I, Corcos O, Couvelard A, Sauvanet A, Rebours V, Vullierme MP, Hentic O, Hammel P, Lévy P, Ruszniewski P. Prevalence of extrapancreatic cancers in patients with histologically proven intraductal papillary mucinous neoplasms of the pancreas: a case-control study. Am J Gastroenterol. 2008;103:2878–2882. [PubMed]
23. Ishida M, Egawa S, Kawaguchi K, Aoki T, Sakata N, Mikami Y, Motoi F, Abe T, Fukuyama S, Katayose Y, et al. Synchronous and metachronous extrapancreatic malignant neoplasms in patients with intraductal papillary-mucinous neoplasm of the pancreas. Pancreatology. 2008;8:577–582. [PubMed]
24. Eguchi H, Ishikawa O, Ohigashi H, Tomimaru Y, Sasaki Y, Yamada T, Tsukuma H, Nakaizumi A, Imaoka S. Patients with pancreatic intraductal papillary mucinous neoplasms are at high risk of colorectal cancer development. Surgery. 2006;139:749–754. [PubMed]
25. Salvia R, Partelli S, Crippa S, Landoni L, Capelli P, Manfredi R, Bassi C, Pederzoli P. Intraductal papillary mucinous neoplasms of the pancreas with multifocal involvement of branch ducts. Am J Surg. 2009;198:709–714. [PubMed]
26. Fritz S, Fernandez-del Castillo C, Mino-Kenudson M, Crippa S, Deshpande V, Lauwers GY, Warshaw AL, Thayer SP, Iafrate AJ. Global genomic analysis of intraductal papillary mucinous neoplasms of the pancreas reveals significant molecular differences compared to ductal adenocarcinoma. Ann Surg. 2009;249:440–447. [PubMed]
27. Furukawa T, Klöppel G, Volkan Adsay N, Albores-Saavedra J, Fukushima N, Horii A, Hruban RH, Kato Y, Klimstra DS, Longnecker DS, et al. Classification of types of intraductal papillary-mucinous neoplasm of the pancreas: a consensus study. Virchows Arch. 2005;447:794–799. [PubMed]
28. Ban S, Naitoh Y, Mino-Kenudson M, Sakurai T, Kuroda M, Koyama I, Lauwers GY, Shimizu M. Intraductal papillary mucinous neoplasm (IPMN) of the pancreas: its histopathologic difference between 2 major types. Am J Surg Pathol. 2006;30:1561–1569. [PubMed]

Articles from World Journal of Gastrointestinal Surgery are provided here courtesy of Baishideng Publishing Group Inc