Article
Macrothrombocytopenia with leukocyte inclusions in a patient with Wilson disease: a case report and literature review.
BMC medical genomics - 17 Jul 2024
Lin Shaoze, Cai Jianling, Huang Yuxuan, Chen Hongxing, Yu Meidie, Zhang Dongqing, Huang Zhanqin
Abstract excerpt
BACKGROUND: Wilson disease (WD) is an autosomal recessive disorder caused by homozygous or compound heterozygous mutations in ATP7B. Clinical manifestations primarily involve liver and nervous system lesions, with rarely observed hematologic manifestations. CASE PRESENTATION: In the present case, a patient with WD presented with thrombocytopenia, giant platelets, and Döhle-like cytoplasmic inclusions in the...
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