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BMC Med Genomics ; 17(1): 188, 2024 Jul 17.
Article in English | MEDLINE | ID: mdl-39020387

ABSTRACT

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 leukocytes. Initially, the May-Hegglin anomaly was considered; however, whole-exome sequencing did not reveal any mutation in the MYH9 gene but a heterozygous mutation was found in (C.2804 C > T, p.T935M) in the ATP7B gene. After two years, the patient developed tremors in his hands, lower limb stiffness, and foreign body sensation in the eyes. Additionally, Kayser-Fleischer rings in the corneal limbus were detected by slit-lamp examination. Copper metabolism test indicated a slight decrease in serum ceruloplasmin. Transmission electron microscopy revealed that the inclusion bodies of leukocytes were swollen mitochondria. Mass spectrometry analysis showed that the copper levels were almost 20-fold higher in the leukocytes of the patient than in those of the control group. Based on the Leipzig scoring system, a diagnosis of WD was confirmed. Zinc sulfate treatment ameliorated the patient's symptoms and enhanced platelet, serum ceruloplasmin, and albumin levels. CONCLUSIONS: In conclusion, this case represents the first documented instance of WD presenting as thrombocytopenia, giant platelets, and Döhle-like cytoplasmic inclusions in the leukocytes. Excessive cellular copper accumulation likely underlies these findings; however, understanding precise mechanisms warrants further investigation.


Subject(s)
Hepatolenticular Degeneration , Inclusion Bodies , Leukocytes , Thrombocytopenia , Humans , Copper-Transporting ATPases/genetics , Copper-Transporting ATPases/metabolism , Hepatolenticular Degeneration/pathology , Hepatolenticular Degeneration/genetics , Hepatolenticular Degeneration/complications , Inclusion Bodies/pathology , Inclusion Bodies/metabolism , Leukocytes/pathology , Leukocytes/metabolism , Mutation , Thrombocytopenia/pathology
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