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Article: Inflammatory fibroid polyps of gastro-intestinal tract

TitleInflammatory fibroid polyps of gastro-intestinal tract
Authors
KeywordsGastrointestinal Tract
Immunohistochemistry
Inflammatory Fibroid Polyps
Issue Date2000
Citation
Chinese Journal of Cancer Research, 2000, v. 12 n. 2, p. 138-140 How to Cite?
AbstractObjective: To review the diagnosis and differential diagnosis of inflammatory fibroid polyp (IFP) of gastrointestinal tract. Methods: The clinical symptoms, histopathologic features and immunohistochemical (ABC method) staining in 9 cases were observed. Results: IFP presented either as a solitary pedunculated or sessile lesion arising from the submucosa and protroding into the lumen; composed of a background of fibroblasts and blood vessels infiltrated by a variable number of inflammatory cells, often numerous eosinophilias leukocytes. Immunohistochemical staining: the spindle cells of all cases reacted with Vimentin. The partial cells of several cases react with Actin, NSE, α AT. 7 cases were follow-up. No patients had a recurrence of the lesion. Conclusion: IFP are rare lesions, and may represent an exaggerated response to inflammatory or other injury process. The prognosis is good when treated by segmental resections of endoscopic removals.
Persistent Identifierhttp://hdl.handle.net/10722/91177
ISSN
2015 Impact Factor: 2.201
2015 SCImago Journal Rankings: 0.727

 

DC FieldValueLanguage
dc.contributor.authorMeng, F-Qen_HK
dc.contributor.authorQian, C-Yen_HK
dc.contributor.authorHuang, Zen_HK
dc.date.accessioned2010-09-17T10:14:15Z-
dc.date.available2010-09-17T10:14:15Z-
dc.date.issued2000en_HK
dc.identifier.citationChinese Journal of Cancer Research, 2000, v. 12 n. 2, p. 138-140en_HK
dc.identifier.issn1000-9604en_HK
dc.identifier.urihttp://hdl.handle.net/10722/91177-
dc.description.abstractObjective: To review the diagnosis and differential diagnosis of inflammatory fibroid polyp (IFP) of gastrointestinal tract. Methods: The clinical symptoms, histopathologic features and immunohistochemical (ABC method) staining in 9 cases were observed. Results: IFP presented either as a solitary pedunculated or sessile lesion arising from the submucosa and protroding into the lumen; composed of a background of fibroblasts and blood vessels infiltrated by a variable number of inflammatory cells, often numerous eosinophilias leukocytes. Immunohistochemical staining: the spindle cells of all cases reacted with Vimentin. The partial cells of several cases react with Actin, NSE, α AT. 7 cases were follow-up. No patients had a recurrence of the lesion. Conclusion: IFP are rare lesions, and may represent an exaggerated response to inflammatory or other injury process. The prognosis is good when treated by segmental resections of endoscopic removals.en_HK
dc.languageengen_HK
dc.relation.ispartofChinese Journal of Cancer Researchen_HK
dc.subjectGastrointestinal Tracten_HK
dc.subjectImmunohistochemistryen_HK
dc.subjectInflammatory Fibroid Polypsen_HK
dc.titleInflammatory fibroid polyps of gastro-intestinal tracten_HK
dc.typeArticleen_HK
dc.identifier.emailQian, C:cmqian@hku.hken_HK
dc.identifier.authorityQian, C=rp1371en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.scopuseid_2-s2.0-0033948517en_HK
dc.identifier.volume12en_HK
dc.identifier.issue2en_HK
dc.identifier.spage138en_HK
dc.identifier.epage140en_HK

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