Wilson’s Disease with Lymphoproliferative Disorder: A Case Report

Jha, Ashish; Sah, Saroj Kumar; Pradhan, Ravi Ranjan

Publication:
Wilson’s Disease with Lymphoproliferative Disorder: A Case Report

creativeworkseries.issn	JNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X
dc.contributor.author	Jha, Ashish
dc.contributor.author	Sah, Saroj Kumar
dc.contributor.author	Pradhan, Ravi Ranjan
dc.date.accessioned	2025-07-28T07:09:45Z
dc.date.available	2025-07-28T07:09:45Z
dc.date.issued	2025
dc.description	Ashish Jha Madhesh Institute of Health Sciences, Janakpurdham, Dhanusha, Nepal Saroj Kumar Sah Kanti Childrens’ Hospital, Maharajgunj, Kathmandu, Nepal Ravi Ranjan Pradhan Beni Provincial Hospital, Beni, Myagdi, Nepal
dc.description.abstract	Abstract Wilson's disease is characterized by copper accumulation in organs like liver, brain, and eyes, presenting with a varied clinical features, making it challenging to diagnose. This report describes a case of Wilson’s disease with unusual hematological features. A 12-year-old from Himalayan region presented with weakness, dysarthria, tremors. Initial investigations revealed pancytopenia, and bone marrow showed a lymphoproliferative disorder. He developed behavioral changes, a flat affect, and scanning speech. Wilson’s disease was confirmed through Kayser-Fleischer rings, reduced serum ceruloplasmin levels, and elevated urinary copper, supported by imaging.
dc.identifier	https://doi.org/10.31729/jnma.8983
dc.identifier.uri	https://hdl.handle.net/20.500.14572/812
dc.language.iso	en_US
dc.publisher	Nepal Medical Association
dc.title	Wilson’s Disease with Lymphoproliferative Disorder: A Case Report
dc.type	Other
dspace.entity.type	Publication
local.article.type	Case Report
oaire.citation.endPage	342
oaire.citation.startPage	340
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