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A thirteen year old female with primary T-cell rich B-cell lymphoma of bone masquerading as chronic recurrent multifocal osteomyelitis

机译:一名13岁女性,其原发性T细胞丰富的B细胞淋巴瘤被假装为慢性复发性多灶性骨髓炎

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Primary lymphoma of the bone (PLB) accounts for 2% of all non-Hodgkin’s lymphomas, and until recently it had not been well characterized in literature. Most cases present in adulthood (average age 50), with localized painful lesions in the long bones, cranium, or axial skeleton. We describe a case of multifocal PLB in an adolescent female. In this case, the initial presentation, with migratory large joint polyarthralgias and bone pain, mimicked chronic recurrent multifocal osteomyelitis (CRMO). Had a biopsy not been performed the diagnosis would have been missed.
机译:骨原发性淋巴瘤(PLB)占所有非霍奇金淋巴瘤的2%,直到最近它在文献中还没有得到很好的表征。大多数病例在成年期(平均年龄为50岁)出现,长骨,头盖骨或轴向骨骼局部疼痛。我们描述了一个青春期女性多灶性小脑的病例。在这种情况下,最初的表现是迁徙性大关节多关节痛和骨痛,模仿了慢性复发性多灶性骨髓炎(CRMO)。如果不进行活检,诊断将被漏诊。

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