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Article: Solid-cystic papillary tumor of the pancreas in children

TitleSolid-cystic papillary tumor of the pancreas in children
Authors
KeywordsAsian
Children
Solid-cystic papillary tumor of the pancreas
Issue Date2001
PublisherSpringer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/00383/index.htm
Citation
Pediatric Surgery International, 2001, v. 17 n. 8, p. 614-620 How to Cite?
AbstractSolid-cystic papillary tumor (SCPT) of the pancreas is a rare neoplasm in children. The current study attempted to estimate the incidence and possible pathological origin of the tumor. Clinicopathologic features of the children under the age of 16 years with pancreatic tumors managed in a single institution between January 1993 and November 1999 were reviewed. Representative blocks of SCPT specimens were immunostained for neuron-specific enolase (NSE) chromogrannin, synaptophysin, insulin, glucagon, somatostatin, and gastrin. There were three SCPTs, two pancreatic endocrine tumors, and one acinar cell carcinoma during the study period. The estimated yearly incidence in the referral area of 2 million population is about 0.01 pediatric SCPT per year per 100,000 population. The children underwent surgical removal of the tumors. Postoperatively, they were followed up for 6 months to 4 years and were well. Immunostaining for NSE, chromogranin, synaptophysin, insulin, somatostatin, and gastrin was negative in all cases. SCPT may thus be the most common pancreatic tumor in the Asian pediatric population. The pathological origin of the tumor remains unclear and requires further investigations.
Persistent Identifierhttp://hdl.handle.net/10722/72325
ISSN
2015 Impact Factor: 1.01
2015 SCImago Journal Rankings: 0.409
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorZhou, Hen_HK
dc.contributor.authorCheng, Wen_HK
dc.contributor.authorLam, KYen_HK
dc.contributor.authorChan, GCFen_HK
dc.contributor.authorKhong, PLen_HK
dc.contributor.authorTam, PKHen_HK
dc.date.accessioned2010-09-06T06:40:31Z-
dc.date.available2010-09-06T06:40:31Z-
dc.date.issued2001en_HK
dc.identifier.citationPediatric Surgery International, 2001, v. 17 n. 8, p. 614-620en_HK
dc.identifier.issn0179-0358en_HK
dc.identifier.urihttp://hdl.handle.net/10722/72325-
dc.description.abstractSolid-cystic papillary tumor (SCPT) of the pancreas is a rare neoplasm in children. The current study attempted to estimate the incidence and possible pathological origin of the tumor. Clinicopathologic features of the children under the age of 16 years with pancreatic tumors managed in a single institution between January 1993 and November 1999 were reviewed. Representative blocks of SCPT specimens were immunostained for neuron-specific enolase (NSE) chromogrannin, synaptophysin, insulin, glucagon, somatostatin, and gastrin. There were three SCPTs, two pancreatic endocrine tumors, and one acinar cell carcinoma during the study period. The estimated yearly incidence in the referral area of 2 million population is about 0.01 pediatric SCPT per year per 100,000 population. The children underwent surgical removal of the tumors. Postoperatively, they were followed up for 6 months to 4 years and were well. Immunostaining for NSE, chromogranin, synaptophysin, insulin, somatostatin, and gastrin was negative in all cases. SCPT may thus be the most common pancreatic tumor in the Asian pediatric population. The pathological origin of the tumor remains unclear and requires further investigations.en_HK
dc.languageengen_HK
dc.publisherSpringer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/00383/index.htmen_HK
dc.relation.ispartofPediatric Surgery Internationalen_HK
dc.subjectAsianen_HK
dc.subjectChildrenen_HK
dc.subjectSolid-cystic papillary tumor of the pancreasen_HK
dc.subject.meshAdolescenten_HK
dc.subject.meshAsian Continental Ancestry Groupen_HK
dc.subject.meshChilden_HK
dc.subject.meshCystadenoma, Papillary - diagnosis - ethnology - pathologyen_HK
dc.subject.meshFemaleen_HK
dc.subject.meshHumansen_HK
dc.subject.meshMagnetic Resonance Imagingen_HK
dc.subject.meshMaleen_HK
dc.subject.meshPancreatic Neoplasms - diagnosis - ethnology - pathologyen_HK
dc.subject.meshPrognosisen_HK
dc.subject.meshRetrospective Studiesen_HK
dc.titleSolid-cystic papillary tumor of the pancreas in childrenen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0179-0358&volume=17&spage=614&epage=620&date=2001&atitle=Solid-cystic-papillary+tumor+of+the+pancreas+in+childrenen_HK
dc.identifier.emailChan, GCF:gcfchan@hkucc.hku.hken_HK
dc.identifier.emailKhong, PL:plkhong@hkucc.hku.hken_HK
dc.identifier.emailTam, PKH:paultam@hkucc.hku.hken_HK
dc.identifier.authorityChan, GCF=rp00431en_HK
dc.identifier.authorityKhong, PL=rp00467en_HK
dc.identifier.authorityTam, PKH=rp00060en_HK
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1007/s003830100005en_HK
dc.identifier.pmid11727051-
dc.identifier.scopuseid_2-s2.0-0035208581en_HK
dc.identifier.hkuros68850en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0035208581&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume17en_HK
dc.identifier.issue8en_HK
dc.identifier.spage614en_HK
dc.identifier.epage620en_HK
dc.identifier.isiWOS:000172735400006-
dc.publisher.placeGermanyen_HK
dc.identifier.scopusauthoridZhou, H=7404741975en_HK
dc.identifier.scopusauthoridCheng, W=7402169228en_HK
dc.identifier.scopusauthoridLam, KY=7403657165en_HK
dc.identifier.scopusauthoridChan, GCF=16160154400en_HK
dc.identifier.scopusauthoridKhong, PL=7006693233en_HK
dc.identifier.scopusauthoridTam, PKH=7202539421en_HK

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