Please use this identifier to cite or link to this item: http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/9608
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dc.contributor.authorAbiharan, P.-
dc.contributor.authorBalagobi, B.-
dc.contributor.authorGobishangar, S.-
dc.contributor.authorSenthuran, R.-
dc.contributor.authorThulasi, T.-
dc.date.accessioned2023-07-11T04:04:39Z-
dc.date.available2023-07-11T04:04:39Z-
dc.date.issued2023-
dc.identifier.urihttp://repo.lib.jfn.ac.lk/ujrr/handle/123456789/9608-
dc.description.abstractIntroduction: Stauffer's syndrome is a rare paraneoplastic non metastatic hepatic dysfunction related to renal cell carcinoma. It is characterized by elevated alkaline phosphatase, erythrocyte sedimentation rate, a-2-globulin, y- glutamyl transferase, thrombocytosis, prolongation of prothrombin time and hepatosplenomegaly, in the absence of hepatic metastasis. A rare variant of it with cholestatic jaundice is described in four cases so far in literature. Clinical presentation: We present a case of a patient presented with features of cholestatic jaundice who was found to have a left sided renal cell carcinoma in the work up. Discussion: This case illustrates the importance of considering paraneoplastic syndromes in mind when working up for patients presenting with hepatic dysfunctions without identifiable causes. Conclusion: This may result in early identification and intervention which will result in better outcome and prolong survival rate.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectStauffer's syndromeen_US
dc.subjectParaneoplastic syndromeen_US
dc.subjectRenal carcinomaen_US
dc.subjectCholestatic jaundiceen_US
dc.subjectBosnaik cystsen_US
dc.titleA case report: A rare case of icteric variant of Stauffer's syndromeen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.1016/j.ijscr.2023.108455en_US
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