İntrapulmoner Paraganglioma

dc.authoridAsuman Kilitçi / 0000-0002-5489-2222
dc.contributor.authorKilitçi, Asuman
dc.contributor.authorYılmaz, Fahri
dc.contributor.authorKılıçgün, Hacı Ali
dc.date.accessioned2023-07-14T13:03:22Z
dc.date.available2023-07-14T13:03:22Z
dc.date.issued2021
dc.departmentTıp Fakültesi
dc.description.abstractSir, Paragangliomas are rare tumors originating from paraganglionic tissue that extends from the skull base to the pelvic diaphragm. Although they can be asymptomatic, they can also cause symptoms by secreting catecholamines or with local expansion. They can also be the component of many hereditary diseases. These tumors are reported in various rare localisations, which include lung parenchyma.1 The first primary pulmonary paraganglioma (PP) case was reported by Heppleston in 1958.2 The number of cases diagnosed till date is less than 50 in the English literature.en_US
dc.identifier.citationKilitci, A., Yilmaz, F., & Kilicgun, H. A. (2021). Intrapulmonary Paraganglioma. Journal of the College of Physicians and Surgeons Pakistan, 31(10), 1253-1255.en_US
dc.identifier.doi10.29271/jcpsp.2021.10.1253
dc.identifier.endpage1254en_US
dc.identifier.issn1022-386X
dc.identifier.issn1681-7168
dc.identifier.issue10en_US
dc.identifier.pmid34601857
dc.identifier.scopus2-s2.0-85116653263
dc.identifier.scopusqualityQ2
dc.identifier.startpage1253en_US
dc.identifier.urihttps://doi.org/10.29271/jcpsp.2021.10.1253
dc.identifier.urihttps://hdl.handle.net/20.500.12513/5223
dc.identifier.volume31en_US
dc.identifier.wosWOS:000704374800028
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherColl Physıcıans & Surgeons Pakıstanen_US
dc.relation.ispartofJcpsp-Journal Of The College Of Physıcıans And Surgeons Pakıstan
dc.relation.publicationcategoryDiğer
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleİntrapulmoner Paragangliomaen_US
dc.typeLetter

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