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首页> 外文期刊>Journal of Medical Case Reports >Classical Hodgkin lymphoma masquerading as chronic recurrent multifocal osteomyelitis: a case report
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Classical Hodgkin lymphoma masquerading as chronic recurrent multifocal osteomyelitis: a case report

机译:伪装成慢性复发性多灶性骨髓炎的经典霍奇金淋巴瘤1例

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BackgroundHodgkin lymphoma is a hematologic malignancy usually confined to lymphatic structures and commonly associated with constitutional symptoms. Bony involvement and musculoskeletal symptoms are uncommon and typically seen in advanced disease. In this case, we report an unusual presentation of classical Hodgkin lymphoma and highlight diagnostic challenges leading to the misdiagnosis and treatment as chronic recurrent multifocal osteomyelitis. Case presentationA 38-year-old white man presented with lower extremity musculoskeletal pain. Imaging studies revealed multifocal lytic and sclerotic osseous axial lesions. Multiple core needle bone marrow and excisional lymph node biopsies were non-diagnostic. Having met the criteria, a tentative diagnosis of chronic recurrent multifocal osteomyelitis was given. He was treated with non-steroidal anti-inflammatory medications with partial clinical response but had persistent symptoms. A second medical opinion was pursued. An open bone marrow biopsy was performed and yielded a diagnosis of classical Hodgkin lymphoma after 13 months of diagnostic uncertainty. A chemotherapy regimen of doxorubicin, bleomycin, vinblastine, and dacarbazine was instituted with complete symptomatic and radiologic response. ConclusionsThis case illustrates diagnostic difficulties of a musculoskeletal presentation of Hodgkin lymphoma, challenges of non-diagnostic bone marrow and lymph node biopsies, and resultant diagnostic delays in delivering a potentially curative therapy. Had the additional open bone marrow biopsy not been performed, the diagnosis and treatment of Hodgkin lymphoma would have been missed.
机译:背景霍奇金淋巴瘤是一种血液恶性肿瘤,通常局限于淋巴结构,通常与体质症状相关。骨受累和肌肉骨骼症状不常见,通常见于晚期疾病。在这种情况下,我们报告了典型的霍奇金淋巴瘤的异常表现,并突出了诊断挑战,导致作为慢性复发性多灶性骨髓炎的误诊和治疗。病例介绍一名38岁的白人患有下肢肌肉骨骼疼痛。影像学检查显示多灶性溶解性和硬化性骨性轴向病变。多中心针头骨髓和切除淋巴结活检未确诊。符合标准后,可对慢性复发性多灶性骨髓炎进行初步诊断。他接受了部分临床反应的非甾体类抗炎药治疗,但症状持续。寻求第二种医学意见。经过13个月的诊断不确定性后,进行了开放式骨髓活检,并诊断为经典霍奇金淋巴瘤。建立了对阿霉素,博来霉素,长春碱和达卡巴嗪的化疗方案,该方案具有完全的症状和放射学反应。结论该病例说明了霍奇金淋巴瘤的肌肉骨骼表现的诊断困难,非诊断性骨髓和淋巴结活检的挑战以及提供潜在治愈性治疗的诊断延迟。如果不进行额外的开放式骨髓活检,则霍奇金淋巴瘤的诊断和治疗将被错过。

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