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1 otential (for example, intraductal papillary mucinous neoplasms).
2 ement of patients with Intraductal Papillary Mucinous Neoplasms.
3 the mouse pancreas and prevents formation of mucinous neoplasms.
4 use pancreas to induce intraductal papillary mucinous neoplasms.
5 s on the treatment of intraductal pancreatic mucinous neoplasms.
6 adenocarcinoma, 17 had intraductal papillary mucinous neoplasms, 26 had symptomatic chronic pancreati
7 ndocrine tumors (35%), intraductal papillary mucinous neoplasms (33%), solid pseudopapillary neoplasm
8 amples of 169 PCLs (90 intraductal papillary mucinous neoplasms, 43 mucinous cystic neoplasms, and 36
9 s cystic neoplasm =16, intraductal papillary mucinous neoplasm = 5, neuroendocrine tumors = 4), or 10
10 = 4), or 10 malignant (intraductal papillary mucinous neoplasm = 7, cystadenocarcinomas = 3) lesions.
12 carcinoma arising from intraductal papillary mucinous neoplasms (A-IPMN) and pancreatic ductal adenoc
13 28, borderline 7), 22 intraductal papillary mucinous neoplasms (adenoma 9, borderline 9, cancer 4),
14 s for the treatment of intraductal papillary mucinous neoplasm and cystic lesions of the pancreas app
16 esection of pancreatic intraductal papillary mucinous neoplasm and to correlate recurrence and surviv
17 ntified in 85 HRIs (82 intraductal papillary mucinous neoplasms and 3 pancreatic endocrine tumors).
18 asia in less than 3 cm intraductal papillary mucinous neoplasms and in multiple intraepithelial neopl
19 ucinous cysts, such as intraductal papillary mucinous neoplasms and mucinous cystic neoplasms, have t
20 leads to predominantly intraductal papillary mucinous neoplasms and mucinous cystic neoplasms, while
21 rs, two Brenner tumors not associated with a mucinous neoplasm, and two atypical proliferative (borde
22 omas, 23 as noninvasive proliferative cystic mucinous neoplasms, and only 7 as cystadenocarcinomas.
23 us cystic neoplasm and intraductal papillary mucinous neoplasm are superior to the original 2006 guid
29 lassified 113 resected intraductal papillary mucinous neoplasms as invasive carcinoma (n = 40) or as
30 tations, and high-risk intraductal papillary mucinous neoplasm, as they are at high risk of developin
32 ho underwent "curative" resection for cystic mucinous neoplasms at Mayo Clinic Rochester from 1940 to
33 (</=30 mm) branch-duct intraductal papillary mucinous neoplasm (BD IPMN; 67%), whereas also being spe
34 ients with branch duct intraductal papillary mucinous neoplasms (BD-IPMN) are offered indefinite surv
35 f low-risk branch duct intraductal papillary mucinous neoplasms (BD-IPMNs) has not been established y
38 ology should be retained for both serous and mucinous neoplasms because of the risk of extraovarian i
40 nous cystic neoplasms, intraductal papillary mucinous neoplasm, cystic neuroendocrine tumors, and cys
41 inous cystic neoplasms+intraductal papillary mucinous neoplasms) from benign cystic lesions (serous c
44 for the management of intraductal papillary mucinous neoplasm (IPMN) and mucinous cystic neoplasm we
45 e relationship between intraductal papillary mucinous neoplasm (IPMN) and the developmental ductal va
46 nt of branch duct (BD) intraductal papillary mucinous neoplasm (IPMN) espouse safety of observation o
47 ic duct (MPD)-involved intraductal papillary mucinous neoplasm (IPMN) has been established by surgica
48 eatic branch-duct (BD) intraductal papillary mucinous neoplasm (IPMN) is infrequent and that extrapan
53 tic lesions resembling intraductal papillary mucinous neoplasm (IPMN) were observed as early as 2 mon
54 itis (CP), 71 PDAC, 70 intraductal papillary mucinous neoplasm (IPMN), 16 mucinous cystic neoplasm (M
55 s preneoplastic lesion intraductal papillary mucinous neoplasm (IPMN), to find new microRNA (miRNA)-b
61 logic heterogeneity of intraductal papillary mucinous neoplasms (IPMN) complicates the prediction of
62 population of resected intraductal papillary mucinous neoplasms (IPMN) of the pancreas with respect t
63 for the management of intraductal papillary mucinous neoplasms (IPMN) recommend surgical treatment i
64 section for pancreatic intraductal papillary mucinous neoplasms (IPMN) using targeted next-generation
65 (PDAC) may arise from intraductal papillary mucinous neoplasms (IPMN) with malignant transformation,
66 s, 2 cysts/remnants, 4 intraductal papillary mucinous neoplasms (IPMN), 2 adenocarcinomas, 1 low-grad
69 mors (PanNET, n = 42), intraductal papillary mucinous neoplasms (IPMN, n = 20), and ampulla of Vater
70 ignant mucinous cysts (intraductal papillary mucinous neoplasm [IPMN], mucinous cystic neoplasm [MCN]
71 ations are reported in intraductal papillary mucinous neoplasms (IPMNs) and in McCune-Albright syndro
73 AC precursors known as intraductal papillary mucinous neoplasms (IPMNs) and predictors of their patho
78 iagnostic criterion of intraductal papillary mucinous neoplasms (IPMNs) involving the main duct (MD I
79 e and branch-duct (BD) intraductal papillary mucinous neoplasms (IPMNs) is important to understand th
80 e growing awareness of intraductal papillary-mucinous neoplasms (IPMNs) of the pancreas among clinici
82 radiographic imaging, Intraductal Papillary Mucinous Neoplasms (IPMNs) of the pancreas are identifie
84 molecular pathology of intraductal papillary mucinous neoplasms (IPMNs) of the pancreas has not been
88 glycoproteins from 64 intraductal papillary mucinous neoplasms (IPMNs), 55 cyst fluid samples, 104 p
89 increased detection of intraductal papillary mucinous neoplasms (IPMNs), and their management remains
90 s cystadenomas (SCAs), intraductal papillary mucinous neoplasms (IPMNs), mucinous cystic neoplasms (M
94 Some cysts, such as intraductal papillary mucinous neoplasms, mucinous cystic neoplasms, and cysti
96 ucosal hyperplasia and low-grade appendiceal mucinous neoplasm (n = 17), and those with malignant muc
97 stic neoplasms (n=17), intraductal papillary mucinous neoplasms (n=15), serous cystadenomas (n=12), o
98 er, the progression of intraductal papillary mucinous neoplasm of the pancreas (IPMN) in this populat
103 e of CBD dilatation in Intraductal Papillary Mucinous Neoplasms of the pancreas (IPMN) among patients
104 carcinomas arising in intraductal papillary mucinous neoplasms of the pancreas (IPMN) by histologica
106 Current understanding is that all cystic mucinous neoplasms of the pancreas are potentially malig
107 f 84 patients (70 women, 14 men) with cystic mucinous neoplasms of the pancreas, 54 were classified a
109 esions (ie, high-grade intraductal papillary mucinous neoplasms or grade 3 pancreatic intraepithelial
115 contrast, noninvasive intraductal papillary mucinous neoplasm recurs infrequently after resection, a
116 a larger proportion of intraductal papillary mucinous neoplasms-related tumors (4/58, 6.9%) than non-
117 itonei (PMP) originating from an appendiceal mucinous neoplasm remains a biologically heterogeneous d
119 s of the treatment of intraductal pancreatic mucinous neoplasms shed some light on the management of
121 fluid from pancreatic intraductal papillary mucinous neoplasms, the monoclonal antibody Das-1 identi
122 Smad4 both regulate an intraductal papillary mucinous neoplasm-to-PDAC sequence through distinct tumo
123 g malignant pancreatic intraductal papillary mucinous neoplasms were developed based on logistic regr
124 sor neoplasms, such as intraductal papillary mucinous neoplasms with high-grade dysplasia and some en
125 ia, or intestinal-type intraductal papillary mucinous neoplasms with intermediate-grade dysplasia.
126 ative R0 microinvasive intraductal papillary mucinous neoplasms (without recurrence at 27, 29, and 34