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dc.contributor.authorTheodosopoulos, Theodosiosen
dc.contributor.authorKarakatsanis, A.en
dc.contributor.authorYiallourou, Anneza I.en
dc.contributor.authorNikolakopoulos, Fotiosen
dc.contributor.authorPsychogiou, Vassilikien
dc.contributor.authorKarvouni, Helenen
dc.contributor.authorVoros, Dionysiosen
dc.creatorTheodosopoulos, Theodosiosen
dc.creatorKarakatsanis, A.en
dc.creatorYiallourou, Anneza I.en
dc.creatorNikolakopoulos, Fotiosen
dc.creatorPsychogiou, Vassilikien
dc.creatorKarvouni, Helenen
dc.creatorVoros, Dionysiosen
dc.date.accessioned2018-06-22T09:53:21Z
dc.date.available2018-06-22T09:53:21Z
dc.date.issued2013
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41791
dc.description.abstractCastleman's disease is a distinct form of lymph node hyperplasia divided into a solitary and a multicentric type. The solitary type occurs most commonly in the mediastinum and is usually asymptomatic. We present a patient with Castleman's disease of the hyaline-vascular solitary type located in the retroperitoneum. The patient was a 38-year-old male, who presented to our hospital with fever. The imaging workup revealed a retroperitoneal mass, measuring 4 × 6 cm, located lateral to the aorta, inferior to the left renal artery and vein, and posterior to the left testicular vein. At workup, a solid hepatic lesion, 3 cm in diameter, located in the left lobe of the liver, segment IV, was also identified. Both lesions were surgically excised. The retroperitoneal tumor had the features of angiofollicular hyperplasia (Castleman's disease), hyaline-vascular type, whereas a diagnosis of focal nodular hyperplasia wasmade for the hepatic lesion. The patient is well at fourty months followup postoperatively. Surgical excision is the treatment of choice for unifocal Castleman's disease. ABSTRACT FROM AUTHOR]; Copyright of Case Reports in Surgery is the property of Hindawi Limited and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)en
dc.sourceCase Reports in Surgeryen
dc.source.urihttp://search.ebscohost.com/login.aspx?direct=true&db=a9h&AN=94854941&site=ehost-live
dc.subjectCastleman's diseaseen
dc.subjectComorbidityen
dc.subjectFeveren
dc.subjectHyperplasiaen
dc.subjectLymph node diseasesen
dc.subjectRare diseasesen
dc.subjectRetroperitoneum diseasesen
dc.titleA Rare Coexistence of Retroperitoneal Pararenal Castleman's Disease with Focal Nodular Hyperplasiaen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1155/2013/537593
dc.description.startingpage1
dc.description.endingpage4
dc.author.facultyΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidYiallourou, Anneza I. [0000-0003-1237-1661]
dc.contributor.orcidKarakatsanis, A. [0000-0002-5509-8645]
dc.gnosis.orcid0000-0003-1237-1661
dc.gnosis.orcid0000-0002-5509-8645


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