Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1991-4-16
pubmed:abstractText
Papillary cystic tumor of the pancreas almost always occurs in young female patient and metastasis is extremely rare although local recurrence may occur. Prognosis is excellent and the tumor can be considered to be curable by surgery. Reported here is an unusual case of malignant papillary cystic tumor of the pancreas that occurred in a 51 Y/O man with metastasis to bilateral inguinal soft tissue at the time of diagnosis. Beside distal pancreatectomy, subtotal gastrectomy and excision of the inguinal masses were also performed because of the presence of a separate tumor in the lesser sac, which was unrelated to the pancreas. Immunohistochemical staining for NSE was positive in tumor cells. However, electron microscopy failed to reveal neurosecretory or zymogen granules but there were abundant mitochondria, rough endoplasmic reticulum and annulate lamellae. These findings show that a ductal origin is more likely in our case but the hypothesis of an origin from a primitive cell capable of acinar, ductal or endocrine differentiation should also be considered.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0578-1337
pubmed:author
pubmed:issnType
Print
pubmed:volume
47
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
139-44
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed:year
1991
pubmed:articleTitle
Malignant papillary cystic tumor of the pancreas: report of a case and review of the literature.
pubmed:affiliation
Department of Pathology, Veterans General Hospital-Taichung, Taiwan, R.O.C.
pubmed:publicationType
Journal Article, Case Reports