Please use this identifier to cite or link to this item: http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/11162
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dc.contributor.authorJenosha, I.-
dc.contributor.authorKumanan, T.-
dc.contributor.authorSuganthan, N.-
dc.contributor.authorSooriyakumar, T.-
dc.contributor.authorPranja, G.-
dc.date.accessioned2025-03-17T03:37:45Z-
dc.date.available2025-03-17T03:37:45Z-
dc.date.issued2025-
dc.identifier.citationAsian J Intern Med. 2025 Jan-Feb; 4(1)en_US
dc.identifier.urihttp://repo.lib.jfn.ac.lk/ujrr/handle/123456789/11162-
dc.description.abstractAcute lymphoblastic leukaemia (ALL) typically presents with symptoms of bone marrow failure. Acute hepatitis is a rare and atypical presentation. We report the case of a 16-years old healthy boy, who presented with elevated liver enzymes and jaundice. His Initial investigations ruled out common infectious aetiology of hepatitis. Despite symptomatic management, the patient had persistent bicytopenia, prompting further evaluation with bone marrow biopsy which confirmed CD10-positive B-cell ALL. This case report illustrates the importance of a pragmatic approach to a non-resolving hepatitis.en_US
dc.language.isoenen_US
dc.publisherSri Lanka College of Internal Medicineen_US
dc.subjectAcute B-cell lymphoblastic leukaemiaen_US
dc.subjectAcute hepatitisen_US
dc.titleAcute B-cell lymphoblastic leukaemia presenting as acute hepatitisen_US
dc.typeArticleen_US
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