Please use this identifier to cite or link to this item: http://20.193.157.4:9595/xmlui/handle/123456789/1017
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dc.contributor.authorK Mamatha, M H Karigoudar, K V Sathyashree, Anil Reddy Konduru, Balasaheb R Yelikar.-
dc.date.accessioned2019-10-14T05:37:19Z-
dc.date.available2019-10-14T05:37:19Z-
dc.date.issued2018-08-
dc.identifier.issn0973709X-
dc.identifier.urihttp://hdl.handle.net/123456789/1017-
dc.description.abstractHydatid disease caused by Echinococcus granulosus is a common occurrence in liver and lungs. Isolated renal hydatid cyst without liver or lung involvement is extremely rare. We present a case of solitary renal hydatid disease diagnosed radiologically as a renal malignancy and intraoperatively suspected as a case of renal tuberculosis due to the extensive necrotic material and as the patient was a treated case of pulmonary tuberculosis. Diagnosis of renal hydatid disease was confirmed on histopathologyen_US
dc.language.isoenen_US
dc.publisherBLDE(Deemed to be University)en_US
dc.subjectCytocentrifugation, Hydatid cysten_US
dc.titleIsolated Renal Hydatid Disease-A Cytohistological Diagnosisen_US
dc.typeArticleen_US
Appears in Collections:Faculty of Pathology

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