A Case of Precursor B-cell Acute Lymphoblastic Leukemia Occurre d with Rapid Hip Bone Destruction and Femoral Neck Fracture

Yutaka Suzuki, T. Asano, D. Takahashi, T. Irie, Ryuta Arai, Yuko Cho, A. Iguchi, M. Terkawi, N. Iwasaki
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引用次数: 1

Abstract

Background: Precursor B-cell lymphoblastic lymphoma is a rare subtype of acute lymphoblastic lymphoma and sometimes presents as lytic bone lesions. Diagnosis and treatment of lytic bone lesions are always challenging. This is a rare case of delayed leukemic change of precursor B-cell acute lymphoblastic lymphoma presented with a rapid hip bone destruction. Case presentation: A 12-year-old Japanese girl presented with progressive left hip pain, and bone destruction of her left hip two months after the onset of symptoms. She had no past medical or family history of malignancy and had no genetic abnormality. Radiograph and MRI examination showed bone destruction and osteolytic lesions in her left femoral neck and pelvis. Blast cells were not found in our initial examination of the peripheral blood and aspirated bone marrow cells. The case was finally diagnosed as Precursor B-cell lymphoblastic lymphoma as the results of bone biopsy, and blast cells were then detected after preforming multiple bone marrow aspirations. She also had pathological femoral neck fracture, but after treatment regimen by chemotherapy, her osteolytic lesions cured with obtainment of femoral neck fusion. She could walk at the final period. Conclusion: This case highlights the importance of early diagnosis of this disease for greater curing rates. Diagnosis of Precursor B-cell lymphoblastic lymphoma was finally made based on the results of biopsy of tissues because of the delayed appearance of leukemic changes. Orthopaedic surgeons should be aware of Precursor B-cell lymphoblastic lymphoma, when making diagnosis of patients exhibiting a rapid hip bone destruction.
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前体b细胞急性淋巴细胞白血病伴快速髋部骨破坏及股骨颈骨折1例
背景:前体B细胞淋巴细胞淋巴瘤是一种罕见的急性淋巴细胞淋巴瘤亚型,有时表现为溶解性骨病变。溶解性骨病变的诊断和治疗总是具有挑战性的。这是一个罕见的前体B细胞急性淋巴细胞淋巴瘤的延迟性白血病改变,表现为髋骨快速破坏。病例介绍:一名12岁的日本女孩在出现症状两个月后出现进行性左髋疼痛和左髋骨破坏。她没有恶性肿瘤病史或家族史,也没有遗传异常。射线照片和核磁共振检查显示她的左股骨颈和骨盆有骨质破坏和溶骨性病变。在我们对外周血和吸入骨髓细胞的初步检查中没有发现Blast细胞。根据骨活检结果,该病例最终被诊断为前体B细胞淋巴母细胞淋巴瘤,然后在预形成多个骨髓愿望后检测到母细胞。她也有病理性股骨颈骨折,但经过化疗方案,她的溶骨性病变通过股骨颈融合术治愈。她可以在最后阶段走路。结论:该病例强调了早期诊断该疾病对提高治愈率的重要性。由于白血病改变的延迟出现,最终根据组织活检结果诊断为前体B细胞淋巴细胞淋巴瘤。骨科医生在诊断髋关节骨快速破坏的患者时,应注意前体B细胞淋巴母细胞淋巴瘤。
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