Wang Jia, Fan Shouren, Liu Jie, Song Bao
School of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences; Department of Oncology, Shandong Cancer Hospital affiliated to Shandong University.
School of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences; Department of Intervention, Qihe People's Hospital.
Onco Targets Ther. 2016 Aug 9;9:4923-8. doi: 10.2147/OTT.S108000. eCollection 2016.
Primary bone lymphoma is a rare and peculiar extranodal presentation of non-Hodgkin's lymphoma, which threatens human health. It can be defined as a lymphoma that occurs in the bone, consisting of a single bone lesion with or without regional lymphadenopathies, and its underlying causes are largely unknown. In this case report, we describe a male who presented with left-sided distal forearm pain, swelling of 2 months duration, and progressive limited wrist motion for about 1 month. The patient had no significant medical history except diabetes. Magnetic Resonance Imaging demonstrated a sheet-like bone destruction area in the left-sided radius, localized discontinuous bone cortex, and adjacent soft tissue masses. Finally, a bone biopsy examined by histopathological and immunochemical methods confirmed a diagnosis of primary bone diffuse large B-cell lymphoma. Due to the rarity of this disease, the level of evidence supporting some diagnostic and therapeutic decisions remains low, and therefore, the details of the rare case may facilitate treatment of similar diseases and provide insight about this obscure lymphoproliferative malignancy. Also, related recent literature reports of primary bone lymphoma are reviewed.
原发性骨淋巴瘤是一种罕见且特殊的非霍奇金淋巴瘤的结外表现形式,威胁着人类健康。它可被定义为发生于骨骼的淋巴瘤,由单个骨病变组成,伴有或不伴有区域淋巴结肿大,其潜在病因大多未知。在本病例报告中,我们描述了一名男性患者,他出现左侧前臂远端疼痛、肿胀2个月,且腕关节活动逐渐受限约1个月。该患者除糖尿病外无其他重大病史。磁共振成像显示左侧桡骨有片状骨质破坏区、局限性不连续骨皮质以及相邻软组织肿块。最后,通过组织病理学和免疫化学方法进行的骨活检确诊为原发性骨弥漫性大B细胞淋巴瘤。由于这种疾病罕见,支持某些诊断和治疗决策的证据水平仍然较低,因此,该罕见病例的细节可能有助于类似疾病的治疗,并为这种隐匿的淋巴增殖性恶性肿瘤提供见解。此外,还对原发性骨淋巴瘤的相关近期文献报道进行了综述。