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Precursor B-Lymphoblastic Lymphoma Presenting as a Solitary Bone Tumor Mimicking Osteomyelitis on MRI

机译:前体B淋巴母细胞淋巴瘤表现为模仿BM的孤立性骨肿瘤

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We describe a 22 year-old man with the rare diagnosis of precursor b-lymphoblastic lymphoma involving only the proximal tibia without evidence of leukemia. He presented with right knee pain and swelling of approximately three months duration and nonspecific radiologic findings and was initially treated for osteomyelitis of unknown etiology. Following histologic diagnosis, the patient received surgical excision of the lesion followed by chemotherapy and radiation. The patient was alive without evidence of disease at nine months follow-up. Introduction Primary precursor B-lymphoblastic lymphoma (B-LBL) of bone is an uncommon neoplasm and accounts for less than 10% of cases of lymphoblastic lymphoma (LBL) and less than 1% of primary bone tumors. It usually involves extranodal sites in young adults and occurs most often in the skin [3]. B-LBL presenting as a solitary bone tumor without involvement of blood, bone marrow, or other sites is extremely rare and less than 10 cases of this type have been reported in the English language literature [3,6]. To the best of our knowledge, only 3 cases of B-LBL involving only the tibia have been reported and this represents the fourth case [6]. B-LBL often presents with few specific radiologic and laboratory findings and thus, can be difficult to diagnose and is often not considered in the patient presenting with bone pain. Case Report A 22-year-old man began to have spontaneous pain and swelling of the right knee in May 2002. Suspecting a tendonitis at the insertion of the patellar tendon, he was treated at an outside hospital with non-steroidal anti-inflammatory medications. This treatment relieved some, but not all of the symptoms. Three months later, the patient presented to the clinic in our department complaining of pain involving the right proximal tibia, including the musculature in this area, when he did any weight-bearing activities. Also, he reported occasionally feeling pain at the region of interest, even while at rest. He had Magnetic resonance (MR) images from an outside hospital that showed an irregular, lytic lesion involving the proximal tibia. (Fig. 1)
机译:我们描述了一个22岁的男子,罕见地诊断为仅涉及胫骨近端而没有白血病证据的前体b淋巴细胞淋巴瘤。他表现出大约三个月的持续时间的右膝疼痛和肿胀以及无特异性放射学表现,最初接受了病因不明的骨髓炎的治疗。经过组织学诊断,患者接受了手术切除的病灶,随后进行了化学疗法和放射治疗。在九个月的随访中,该患者还活着,没有疾病的迹象。简介骨原发性前体B淋巴母细胞淋巴瘤(B-LBL)是一种罕见的肿瘤,约占淋巴母细胞淋巴瘤(LBL)病例的10%以下和原发性骨肿瘤的1%以下。它通常涉及青壮年的结外部位,并且最常见于皮肤[3]。 B-LBL表现为孤立的骨肿瘤而无血液,骨髓或其他部位的侵袭极为罕见,英语文献中报道这种类型的病例少于10例[3,6]。据我们所知,仅报道了3例仅涉及胫骨的B-LBL病例,这是第四例[6]。 B-LBL通常表现出很少的放射学和实验室检查结果,因此可能难以诊断,并且在出现骨痛的患者中通常不予考虑。病例报告2002年5月,一名22岁的男子开始自发疼痛并右膝肿胀。怀疑the骨肌腱插入时出现肌腱炎,他在一家外部医院接受非甾体类抗炎药治疗。这种治疗缓解了部分症状,但不是全部。三个月后,该患者在进行任何负重活动时,诉至我科门诊,抱怨疼痛涉及右胫骨近端,包括该区域的肌肉组织。此外,他报告说,即使在休息时,偶尔也会在目标区域感到疼痛。他从一家外部医院获得了磁共振(MR)图像,显示出不规则的溶解性病变累及胫骨近端。 (图。1)

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