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胸椎ALK阳性间变性大细胞淋巴瘤

ALK positive Anaplastic Large Cell Lymphoma of the Thoracic Spine.

作者信息

Abrego Gabriela, García Julio, Gilbert Bruce, Forseen Scott, Toscano Michael

机构信息

Department of Radiology and Imaging, GRU Medical Center, Augusta, Georgia, USA.

Department of Pathology, GRU Medical Center, Augusta, Georgia, USA.

出版信息

J Radiol Case Rep. 2016 Sep 30;10(9):1-12. doi: 10.3941/jrcr.v10i9.2590. eCollection 2016 Sep.

Abstract

Primary bone lymphoma (PBL) is an uncommon extra nodal disease that represents about 1-3% of lymphoma cases. Imaging findings are variable and non-specific. Computed tomography may demonstrate lytic lesions with sequestra and periosteal reaction. On magnetic resonance imaging, lesions are T1WI hypointense and T2WI hyperintense, related to peritumoral edema or bone marrow replacement. Rarely lesions may have associated fibrosis and show a more hypointense signal pattern on T2WI. After administration of contrast, PBL tends to enhance avidly. We present a case of a 24 years old African American female patient with history of back pain. Initial imaging examinations showed lesions involving the T12 and T11 vertebral bodies with initial negative biopsy results. One month later, the patient returned with worsening back pain, and the follow up studies depicted collapse of the T12 vertebral body. A diagnosis of anaplastic large cell lymphoma in T12 was made. A brief review of the literature, imaging and pathological findings, and treatment options are also discussed.

摘要

原发性骨淋巴瘤(PBL)是一种罕见的结外疾病,约占淋巴瘤病例的1%至3%。影像学表现多样且无特异性。计算机断层扫描可能显示伴有死骨和骨膜反应的溶骨性病变。在磁共振成像上,病变在T1加权像上呈低信号,在T2加权像上呈高信号,与瘤周水肿或骨髓替代有关。病变很少会伴有纤维化,在T2加权像上表现为更低信号模式。注射造影剂后,PBL往往会显著强化。我们报告一例24岁非裔美国女性患者,有背痛病史。最初的影像学检查显示病变累及T12和T11椎体,初始活检结果为阴性。一个月后,患者因背痛加重复诊,后续检查显示T12椎体塌陷。最终诊断为T12椎体间变性大细胞淋巴瘤。本文还简要回顾了相关文献、影像学和病理学表现以及治疗选择。

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