Increased risk of neoplasm

Intraductal papillary mucinous neoplasm (IPMN) is a type of tumor that can occur within the cells of the pancreatic duct. IPMN tumors produce mucus, and this mucus can form pancreatic cysts. [Source: Wikipedia ]

May Be Caused by
Abdominal compartment syndrome
Adrenal hyperplasia
Adrenogenital syndrome
Alagille syndrome
Alpha1-antitrypsin deficiency
Alport syndrome
Asphyxiating thoracic dysplasia
Bannayan-Riley-Ruvalcaba syndrome
Basaloid follicular hamartoma
Bazex syndrome
Beckwith-Wiedemann syndrome
Behçet disease
Birt-Hogg-Dubé syndrome
Bloom syndrome
Blue rubber bleb nevus syndrome
Carcinoid syndrome
Carney complex
Carney triad
Castleman disease
Celiac disease
Chédiak-Higashi syndrome
Clark-Howel-Evans-McConnell syndrome
Costello syndrome
Cowden syndrome
Cronkhite-Canada syndrome
De Sanctis-Cacchione syndrome
Diamond-Blackfan syndrome
Disorganization complex
Doege-Potter syndrome
Dubowitz syndrome
Dyskeratosis congenita
Ehlers-Danlos syndrome
Epidermal nevus syndrome
Epidermolysis bullosa
Familial adenomatous polyposis
Fanconi anemia
Fanconi syndrome
Fetal alcohol syndrome
Fetal hydantoin syndrome
Fibrous dysplasia
Frasier syndrome
Gardner syndrome
Glucagonoma syndrome
Glycogen storage disease type 1
Gorlin syndrome
Hardcastle syndrome
Henoch-Schönlein purpura
Hepatic fibrosis-renal cystic disease
Hereditary multiple exostosis
Hereditary nonpolyposis colon cancer
Hyperparathyroidism-jaw tumor syndrome
Incontinentia pigmenti
Kasabach-Merritt syndrome
Klinefelter syndrome
Lambert-Eaton syndrome
Li-Fraumeni cancer family syndrome
Littoral cell angioma
Lynch syndrome
Maffucci syndrome
Male pseudohermaphroditism
Marfan syndrome
Mazabraud syndrome
Meigs syndrome
Metaphyseal chondrodysplasia Shwachman type
Mirizzi syndrome
MSH6 mutation
Muir-Torre syndrome
Multiple endocrine neoplasia syndrome type 1
Multiple endocrine neoplasia syndrome type 2A
Multiple endocrine neoplasia syndrome type 2B
Myasthenic syndrome
N syndrome
Nephrogenic hepatic dysfunction syndrome
Nephrotic syndrome
Neurocutaneous melanosis sequence
Neurofibromatosis type 1
Neurofibromatosis type 2
Niemann-Pick disease
Nijmegen breakage syndrome
Oculo-auriculo-vertebral spectrum
Oral leukoplakia associated with tylosis and esophageal carcinoma
OSLAM syndrome
Osteogenesis imperfecta
Paget disease of bone
Pallister-Hall syndrome
Paraneoplastic syndrome
Perlman syndrome
Persistent müllerian duct syndrome
Peutz-Jeghers syndrome
Pleuropulmonary blastoma-Wilms tumor association
Poland syndrome
Polyostotic fibrous dysplasia
Porphyria cutanea tarda
Richter syndrome
Ring chromosome 13
Rothmund-Thomson syndrome
Rubinstein-Taybi syndrome
Sjögren syndrome
Sotos syndrome
Spondyloepiphyseal dysplasia tarda
Sterno-costo-clavicular hyperostosis
Stewart-Treves syndrome
Sweet syndrome
Syndrome of inappropriate secretion of antidiuretic hormone
Thymic tumor syndrome
Trisomy 21
Trousseau syndrome
Tuberous sclerosis
Tumor lysis syndrome
Turcot syndrome
Turner syndrome
Von Hippel-Lindau disease
WAGR syndrome
Weinberg-Zumwalt syndrome
Werner syndrome
Wilms tumor-multiple lung hamartomas
Wiskott-Aldrich syndrome
WT limb-blood syndrome
X-linked lymphoproliferative syndrome
Xeroderma pigmentosa syndrome
Yellow nail syndrome
Zollinger-Ellison syndrome