Multicystic adenomatoid hamartoma of the pancreas: a hitherto undescribed pancreatic tumor occurring in a 3-year-old boy.

TitleMulticystic adenomatoid hamartoma of the pancreas: a hitherto undescribed pancreatic tumor occurring in a 3-year-old boy.
Publication TypeJournal Article
Year of Publication2008
AuthorsThrall M, Jessurun J, Stelow EB, N Adsay V, Vickers SM, Whitson AK, Saltzman DA, Pambuccian SE
JournalPediatr Dev Pathol
Volume11
Issue4
Pagination314-20
Date Published2008 Jul-Aug
ISSN1093-5266
KeywordsBiomarkers, Cell Proliferation, Child, Preschool, Disease-Free Survival, Hamartoma, Humans, Immunoenzyme Techniques, Keratin-7, Magnetic Resonance Imaging, Male, Pancreas, Pancreatic Diseases, Pancreaticoduodenectomy
Abstract

This report describes an unusual pancreatic tumor in a 3-year-old boy. He presented with abdominal pain secondary to pancreatitis and was found to have a complex, multicystic lesion within the head of the pancreas. He subsequently underwent a pancreatoduodenectomy. Grossly, the mass was 3 cm, multicystic, and well demarcated. Histologically, there were numerous variably sized, dilated ducts lined by tall columnar mucinous cells surrounded by a stroma that exhibited foci of cellular condensations resembling primitive pancreatic mesenchyme. Acinar and endocrine cells were often seen budding into the ducts forming "ductulo-insular bodies." As a result of its superficial resemblance to Stocker type 2 cystic adenomatoid malformation of the lung, we are proposing the name "multicystic adenomatoid hamartoma" for this lesion.

DOI10.2350/07-04-0260.1
Alternate JournalPediatr Dev Pathol
PubMed ID17990924
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