Gaucher disease type 3 presenting with deformation of inferior limbs and bone infarction: A case report

Zakaria Abide, Chaimae Es-Sebbani, Amine Cherraqi, A. Haddad, N. Allali, L. Chat
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Abstract

Introduction: Gaucher disease (GD) is a lysosomal storage disorder characterized by the accumulation of glucocerebroside in various cells throughout the body. Bone infarction is a common and fearsome complication. Case Report: We present the case of a 5-year-old child diagnosed with Gaucher disease type 3, who exhibited deformation of the inferior limbs and bone pain. Upon evaluation, radiographic examination of the limbs revealed a characteristic triangular appearance of the metaphysis and a serpiginous sclerotic area. A magnetic resonance imaging was performed to confirm the diagnosis of bone infarction. Conclusion: Gaucher disease is a complex genetic disorder. Bone involvement is a significant manifestation causing pain, bone crises, deformities. Various imaging techniques can help for an accurate diagnosis and for a timely intervention and prevention of the disease progression.
以下肢变形和骨梗死为表现的戈歇病3型1例
戈谢病(GD)是一种溶酶体贮积性疾病,其特征是糖脑苷在全身各种细胞中积累。骨梗塞是一种常见而可怕的并发症。病例报告:我们提出的病例5岁儿童诊断为戈歇病3型,谁表现出变形的下肢和骨痛。评估后,四肢的x线检查显示干骺端呈特征性三角形外观和蛇形硬化区。行核磁共振成像以证实骨梗死的诊断。结论:戈谢病是一种复杂的遗传性疾病。骨受累是引起疼痛、骨危机、畸形的重要表现。各种成像技术可以帮助准确诊断,及时干预和预防疾病进展。
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