Hu Xianwen, Xiong Wei, Li Shun, Li Xue, Cai Jiong, Wang Pan, Li Dandan
Affiliated Hospital of Zunyi Medical University, Department of Nuclear Medicine, Zunyi, China.
Yinjiang Autonomous County People's Hospital, Department of Medical Imaging, Yinjiang, China.
Front Med (Lausanne). 2022 Aug 4;9:967531. doi: 10.3389/fmed.2022.967531. eCollection 2022.
Plasma cell myeloma (PCM) is a malignant clonal disease of abnormal proliferation of plasma cells, which is the second most common hematological malignancy after leukemia. PCM often diffuses and involves the bones of the whole body, especially the spinal column, ribs, skull, pelvis, and other axial bones and flat bones. Herein, we present a 55-year-old man who came to the hospital seeking medical help for low-back pain and numbness in his lower limbs. Computed tomography (CT) was performed because the clinician suspected that the patient had a herniated disc, and the results showed that the 7 thoracic vertebrae and the 3 lumbar vertebrae showed a low density of bone destruction with "honeycombing" changes. Magnetic resonance imaging (MRI) showed that the corresponding lesions presented long T1 and long T2 signals, and the lesions were significantly enhanced in contrast-enhanced T1WI sequences, and fluoro18-labeled deoxyglucose positron emission tomography/computed tomography (F-FDG PET/CT) showed mild radioactive uptake in the lesions. Based on these imaging findings, the patient was considered for a diagnosis of hemangiomas, and surgery was performed because the affected vertebra was pressing on the spinal cord. However, intraoperative frozen section examination showed that the patient had plasma cell myeloma. Our case study suggests that PCM involving a single thoracic and lumbar spine is rare and should be considered as one of the imaging differential diagnoses of hemangiomas. Moreover, the diagnosis of PCM is difficult when the number of lesions is small, especially when the plasma cell ratio is within the normal reference range in laboratory tests.
浆细胞骨髓瘤(PCM)是一种浆细胞异常增殖的恶性克隆性疾病,是仅次于白血病的第二常见血液系统恶性肿瘤。PCM常呈弥漫性,累及全身骨骼,尤其是脊柱、肋骨、颅骨、骨盆等中轴骨及扁骨。在此,我们报告一名55岁男性,因腰痛和下肢麻木前来医院寻求医疗帮助。由于临床医生怀疑患者患有椎间盘突出症,故进行了计算机断层扫描(CT),结果显示第7胸椎和第3腰椎呈低密度骨质破坏,伴有“蜂窝状”改变。磁共振成像(MRI)显示相应病变呈长T1和长T2信号,在T1WI增强序列中病变明显强化,氟代脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(F-FDG PET/CT)显示病变有轻度放射性摄取。基于这些影像学表现,该患者被考虑诊断为血管瘤,并因受累椎体压迫脊髓而进行了手术。然而,术中冰冻切片检查显示该患者患有浆细胞骨髓瘤。我们的病例研究表明,累及单个胸腰椎的PCM较为罕见,应被视为血管瘤的影像学鉴别诊断之一。此外,当病变数量较少时,尤其是实验室检查中浆细胞比例在正常参考范围内时,PCM的诊断较为困难。