Mihailovic Jasna, Goldsmith Stanley J
Department of Nuclear Medicine, Oncology Institute of Vojvodina, Sremska Kamenica, Serbia; Technical Faculty "Mihajlo Pupin" Zrenjanin, University of Novi Sad, Novi Sad, Serbia.
Division of Nuclear Medicine & Molecular Imaging, New York-Presbyterian Hospital/Weill Cornell Medical Center, New York, NY; Department of Radiology, Weill Cornell Medical College, New York, NY; Department of Medicine, Weill Cornell Medical College, New York, NY.
Semin Nucl Med. 2015 Jan;45(1):16-31. doi: 10.1053/j.semnuclmed.2014.08.002.
Multiple myeloma (MM) is a relatively rare hematologic disorder characterized by proliferation of plasma cells, primarily involving the bone marrow. Extramedullary involvement also occurs with poor prognosis. Asymptomatic plasma cell disorders, monoclonal gammopathy of uncertain significance, and smoldering MM, which do not require therapy, should be distinguished from symptomatic MM, which requires treatment. MM may present with CRAB, elevated Calcium levels, Renal insufficiency, Anemia, and Bone lesions (including lytic lesions and osteopenia), as well as elevated levels of serum M protein or urine M protein or both. Nonsecretory myeloma in which serum and urine M proteins are absent occurs rarely, accounting for 1%-5% of patients with myeloma, but low levels of abnormal immunoglobulins are often present. Staging of patients with MM is done according to the Durie and Salmon criteria based on laboratory testing (determination of hemoglobin, serum calcium, and serum and urine M proteins) and conventional radiography. A variety of diagnostic imaging procedures have been employed to assess the extent of disease in MM and to evaluate the response to treatment as well as provide surveillance for the detection of recurrent disease. These include whole-body x-ray, which despite its limitations is regularly used to detect lytic bone lesions; CT radiography; MRI; and a variety of radionuclide imaging procedures, with (18)F-FDG-PET/CT emerging as the radionuclide procedure of choice. Recently, the Durie-Salmon criteria have been upgrade to the Durie-Salmon PLUS system, which includes (18)F-FDG-PET/CT and MRI of the spine and pelvis.
多发性骨髓瘤(MM)是一种相对罕见的血液系统疾病,其特征为浆细胞增殖,主要累及骨髓。髓外受累也会出现,且预后较差。无症状浆细胞疾病、意义未明的单克隆丙种球蛋白病和冒烟型MM(无需治疗)应与有症状的MM(需要治疗)相区分。MM可能表现为CRAB,即血钙升高、肾功能不全、贫血和骨病变(包括溶骨性病变和骨质减少),以及血清M蛋白或尿M蛋白水平升高或两者均升高。血清和尿中均无M蛋白的非分泌型骨髓瘤很少见,占骨髓瘤患者的1%-5%,但常存在低水平的异常免疫球蛋白。MM患者的分期根据Durie和Salmon标准进行,基于实验室检测(血红蛋白、血清钙以及血清和尿M蛋白的测定)和传统X线摄影。多种诊断成像程序已被用于评估MM疾病的范围、评估治疗反应以及监测复发性疾病的检测。这些包括全身X线检查,尽管有其局限性,但仍经常用于检测溶骨性骨病变;CT扫描;MRI;以及多种放射性核素成像程序,其中(18)F-FDG-PET/CT已成为首选的放射性核素程序。最近,Durie-Salmon标准已升级为Durie-Salmon PLUS系统,该系统包括脊柱和骨盆的(18)F-FDG-PET/CT和MRI。