19845185

Source:http://linkedlifedata.com/resource/pubmed/id/19845185

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0030297, umls-concept:C0205208
pubmed:dateCreated	2009-10-22
pubmed:abstractText	SPN is a rare neoplasm that affects mainly young women. Despite this feature, SPN have been seen in both genders, multiple races, and at a wide range of ages. The genetic mechanism behind the development of SPN is distinct from the more lethal ductal carcinoma of the pancreas. This difference is reflected in the favorable outcome for patients with SPN. Surgery is typically curative in patents with localized disease and possibly in patients with limited metastasis or local extension. No consensus exists on an effective systemic therapy. There are no reliable predictors for disease-specific mortality or recurrence in the minority of patients who develop aggressive disease.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0045335
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0065-3411
pubmed:author	pubmed-author:ReddySushanthS, pubmed-author:WolfgangChristopher LCL
pubmed:issnType	Print
pubmed:volume	43
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	269-82
pubmed:meshHeading	pubmed-meshheading:19845185-Carcinoma, Papillary, pubmed-meshheading:19845185-Diagnosis, Differential, pubmed-meshheading:19845185-Humans, pubmed-meshheading:19845185-Pancreatectomy, pubmed-meshheading:19845185-Pancreatic Neoplasms, pubmed-meshheading:19845185-Prognosis
pubmed:year	2009
pubmed:articleTitle	Solid pseudopapillary neoplasms of the pancreas.
pubmed:affiliation	John L. Cameron Division of Surgical Oncology, The Sol Goldman Pancreatic Cancer Research Center, Department of Surgery, Johns Hopkins Medical Institutions, 606 Blalock Building, 600 North Wolfe Street, Baltimore, MD 21287, USA.
pubmed:publicationType	Journal Article, Review