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dc.contributor.authorYildiz, Levent
dc.contributor.authorKefeli, Mehmet
dc.contributor.authorKose, Behiye
dc.contributor.authorBaris, Sancar
dc.date.accessioned2020-06-21T15:06:56Z
dc.date.available2020-06-21T15:06:56Z
dc.date.issued2009
dc.identifier.issn0256-4947
dc.identifier.issn1319-9226
dc.identifier.urihttps://doi.org/10.4103/0256-4947.51808
dc.identifier.urihttps://hdl.handle.net/20.500.12712/18735
dc.descriptionWOS: 000266946300010en_US
dc.descriptionPubMed: 19318742en_US
dc.description.abstractAlthough involvement of the thyroid gland by amyloid is a relatively common phenomenon, clinically significant enlargement of the thyroid owing to amyloid deposition is an extremely rare occurrence. We describe two cases of amyloid goiter and review the relevant literature. The first case was systemic amyloidosis secondary to familial Mediterranean fever. The second case was a chronic renal failure patient who presented with an enlarged thyroid and upper airway obstructive symptoms. To date, true amyloid goiter secondary to amyloidosis associated with familial Mediterranean fever has only been reported in twelve patients.en_US
dc.language.isoengen_US
dc.publisherK Faisal Spec Hosp Res Centreen_US
dc.relation.isversionof10.4103/0256-4947.51808en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleAmyloid goiter: two cases and a review of the literatureen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume29en_US
dc.identifier.issue2en_US
dc.identifier.startpage138en_US
dc.identifier.endpage141en_US
dc.relation.journalAnnals of Saudi Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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